Biomarker Development for Postoperative Cognitive Impairment in the Elderly (BioCog) (BioCog)

• ClinicalTrials.gov Identifier: NCT02265263
• Recruitment Status: Terminated
• First Posted: October 15, 2014
• Last Update Posted: September 25, 2019
• Sponsor: Charite University, Berlin, Germany
• Collaborator: European Union
• Information provided by (Responsible Party): Claudia Spies, Charite University, Berlin, Germany

Tracking Information

• First Submitted Date: September 23, 2014
• First Posted Date: October 15, 2014
• Last Update Posted Date: September 25, 2019
• Actual Study Start Date: October 2014
• Actual Primary Completion Date: December 2017 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: February 1, 2018)

• Incidence of Delirium [ Time Frame: Participants will be followed for the duration of hospital stay, an expected average of 7 days ]
  Postoperative delirium rate, defined according to Diagnostic and Statistical Manual of Mental Disorders (DSM-V) and/or as ≥ 2 cumulative points in the nursing Delirium Screening Scale (Nu-DESC) and/or a positive Confusion Assessment Method (CAM) and/or Confusion Assessment Method for the Intensive Care Unit (CAM-ICU) score and/or patient chart review that shows descriptions of delirium.
• Incidence of postoperative cognitive deficit (POCD) [ Time Frame: Up to 3 months after the operation ]
  POCD will be measured by a defined Cambridge Neuropsychological Test Automated Battery (CANTAB) POCD will be measured by a defined Cambridge Neuropsychological Test Automated Battery (CANTAB) and paper pencil tests (TMT A und B, Grooved Pegboard) and the Mini - Mental State Examination (MMSE)

Original Primary Outcome Measures (submitted: October 14, 2014)

• Incidence of Delirium [ Time Frame: Participants will be followed for the duration of hospital stay, an expected average of 7 days ]
  Postoperative delirium rate, defined according to Diagnostic and Statistical Manual of Mental Disorders (DSM-V) and as ≥ 2 cumulative points in the nursing Delirium Screening Scale (Nu-DESC)
• Incidence of postoperative cognitive deficit (POCD) [ Time Frame: Up to 3 months after the operation ]
  POCD will be measured by a defined Cambridge Neuropsychological Test Automated Battery (CANTAB)

Current Secondary Outcome Measures (submitted: July 6, 2018)

• Duration of Delirium [ Time Frame: Participants will be followed for the duration of hospital stay, an exspected average of 7 days ]
  • Diagnostic and Statistical Manual of Mental Disorders (DSM-V)
  • Nursing Delirium Screening Scale (Nu-DESC)
  • Intensive Care Delirium Screening Checklist (ICDSC)
  • Delirium Detection Scale (DDS)
  • Confusion Assessment Method for the Intensive Care Unit (CAM-ICU)
  • Confusion Assessment Method (CAM)
  • Chart Review
• Duration of subsyndromal postoperative delirium [ Time Frame: Participants will be followed for the duration of hospital stay, an exspected average of 7 days ]
  Nu-DESC score 1 and/or any criteria suggestive of POD (as described under "Primary Outcome Measures") that do not fulfill DSM-5 criteria for delirium.
• Incidence of subsyndromal postoperative delirium [ Time Frame: Participants will be followed for the duration of hospital stay, an exspected average of 7 days ]
  Nu-DESC score 1 and/or any criteria suggestive of POD (as described under "Primary Outcome Measures") that do not fulfill DSM-5 criteria for Delirium
• Intensive care unit length of stay [ Time Frame: Participants will be followed for the duration of intensive care unit stay, an expected average of 5 days ]
• Hospital length of stay [ Time Frame: Participants will be followed for the duration of hospital stay, an exspected average of 7 days ]
• Postoperative organ complications [ Time Frame: Participants will be followed for the duration of hospital stay, an exspected average of 7 days ]
  Postoperative organ complications are classified according to Clavien - Dindo classification.
• Incidence of postoperative cognitive deficit [ Time Frame: 1 year, 2 years, 5 years after the operation ]
  POCD will be measured by a defined Cambridge Neuropsychological Test Automated Battery (CANTAB), paper pencil tests (TMT A und B, Grooved Pegboard) and the Mini - Mental State Examination (MMSE)
• Socioeconomic characteristics [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
  Study center Berlin: Health economic data according to cost of patient care (The §21 dataset (diagnoses and operation-codes). Hospital costs are calculated according to the Institute for the Hospital Remuneration System (InEK) calculation scheme to compare the refinanced costs in each cost category/cost-center segment from study center Charité. Necessity and indirect costs of medical care (outpatient visits) after hospital stay.
• Health related quality of life [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
  Study center Berlin: Measurement by EQ-5D
• Barthel Index [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
• Instrumental activities of daily living scale [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
• Hand grip strength test [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
• Malnutrition [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
  Mini Nutritional Assessment - Short form, Serum albumin
• Mobility [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
  Timed up and go test
• Neuroimaging Biomarker [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
• Molecular Biomarker [ Time Frame: 3 months ]
• Health related Quality of life [ Time Frame: 3 months, 1 year after the operation ]
  Study center Utrecht: Measurement by EQ-5D
• Socioeconomic characteristics [ Time Frame: 3 months, 1 year after the operation ]
  Study center Utrecht: Health economic data according to direct cost of patient care (inpatient and outpatient stays) and necessity and indirect costs of medical care (outpatient visits) after hospital stay.
• Heart rate variability [ Time Frame: Study center Berlin: Participants will be followed for the duration of hospital stay, an exspected average of 7 days ]
• Light Levels (lux) [ Time Frame: Study center Berlin: Participants will be followed for the duration of hospital stay, an exspected average of 7 days ]
• Light frequencies [ Time Frame: Study center Berlin: Participants will be followed for the duration of hospital stay, an exspected average of 7 days ]
• Depression [ Time Frame: Participants will be followed for the duration of hospital stay, an exspected average of 7 days ]
  Hospital Anxiety and Depression Scale (HADS) (Study Center Utrecht), GDS-15 (Study Center Berlin)
• Anxiety [ Time Frame: Participants will be followed for the duration of hospital stay, an exspected average of 7 days ]
  Faces Anxiety Scale (FAS)
• Electroencephalography (EEG)- Mapping [ Time Frame: At time of surgery ]
  Study center Berlin: EEG with19 electrodes and hypo- and hyperventilation in physiological limits (no patients with neurological pre-existing conditions or proposed neuro-surgery)
• Mortality [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
• Depth of consciousness index [ Time Frame: At time of surgery ]
  Depth of consciousness index measured by processive Electroencephalography and Electromyography (EEG/EMG) -Data (SedLine®)
• Intraoperative cerebral oxymetry [ Time Frame: At time of surgery ]
• Changes of Electroencephalography [ Time Frame: Participants will be followed up until the end of postanesthesia care unit, an exspected average of 2 days ]
  Signals are measured by EEG Monitor and Delir Monitor software
• Depth of sedation [ Time Frame: At time of surgery and Participants will be followed for the duration of intensive care unit stay, an expected average of 5 days ]
  Intraoperatively: Observe´s Assessment of Alertness/Sedation scale (OAA/S) and postoperatievly: Richmond Agitation Sedation Scale (RASS)
• Pain Scales [ Time Frame: 3 months ]
  Perioperatively: Pain sensitivity questionnare; Pain Catastrophing Scale (PCS-GE)(PSQ); Numerische Rating Scale (NRS-V); Behavioural Pain Scale (BPS for ventilated) and BPS-NI (for non-ventilated) patients, Critical-Care Pain Observation Tool (CPOT); Rotterdam Elderly Pain Observation Scale (REPOS); Pupillometry by Neurolight; Intraoperatively: Measurement of the nociceptive flexion reflex threshold (Dolosys Paintracker); Measurement of the pupillary dilation reflex threshold (AlgiScan); Automatic collection of the data of the medication pumps; Multiple blood analysis to measure the plasma-concentrations of anesthetics; Automatic collection of the data of the SED-Line-EEG-Monitor.
• Quality indicators of intensive care unit [ Time Frame: Participants will be followed for the duration of intensive care unit stay, an expected average of 5 days ]
  Study Center Berlin: This endpoint aims to analyse economic effects of the prospective study patients and retrospective control subjects in the intensive care unit that are caused by the implementation of quality indicators in health care.
• Glucosevariability [ Time Frame: At time of surgery and Participants will be followed for the duration of intensive care unit stay, an expected average of 5 days ]
  Measured by Continuous Glucose Monitoring System
• Frailty [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
• Coagulationdisorder of the blood [ Time Frame: 3 months ]
  Kidney marker

Original Secondary Outcome Measures (submitted: October 14, 2014)

• Duration of Delirium [ Time Frame: Participants will be followed for the duration of hospital stay, an exspected average of 7 days ]
  • Diagnostic and Statistical Manual of Mental Disorders (DSM-V)
  • Nursing Delirium Screening Scale (Nu-DESC)
  • Delirium Rating Scale-revised-98 (DRS-R-98)
  • Intensive Care Delirium Screening Checklist (ICDSC)
• Intensive care unit length of stay [ Time Frame: Participants will be followed for the duration of intensive care unit stay, an expected average of 5 days ]
• Hospital length of stay [ Time Frame: Participants will be followed for the duration of hospital stay, an exspected average of 7 days ]
• Postoperative organ complications [ Time Frame: Participants will be followed for the duration of hospital stay, an exspected average of 7 days ]
  Postoperative organ complications are classified according to Clavien - Dindo classification.
• Incidence of postoperative cognitive deficit [ Time Frame: 1 year, 2 years, 5 years after the operation ]
  POCD will be measured by a defined Cambridge Neuropsychological Test Automated Battery (CANTAB)
• Socioeconomic characteristics [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
  Health economic data according to cost of patient care (The §21 dataset (diagnoses and operation-codes) from study centers in Berlin or equivalent Diagnosebehandelcombinatie (DBC)-Code and unit costs from study center in Utrecht). Necessity of medical care after hospital stay.
• Quality of life [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
• Barthel Index [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
• Instrumental activities of daily living scale [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
• Hand grip strength test [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
• Malnutrition [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
  Mini Nutritional Assessment
• Mobility [ Time Frame: 3 months, 1, 2 and 5 years after the operation ]
  Timed up and go test

• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: Biomarker Development for Postoperative Cognitive Impairment in the Elderly (BioCog)
• Official Title: Biomarker Development for Postoperative Cognitive Impairment in the Elderly (BioCog)

Brief Summary

The research leading consortium to these results has received funding from the European Union Seventh Framework Programme [FP7/2007-2013] under grant agreement no 602461 (www.biocog.eu).

The investigators will establish valid biomarkers panels (neuroimaging and molecular) for risk and clinical outcome prediction of postoperative delirium (POD)/postoperative cognitive deficit (POCD) in elective surgical patients (Age ≥ 65 years) in study centers in Berlin,Germany (data collection within 2 years after initial hospital stay) and Utrecht, The Netherlands (data collection within 1 year after initial hospital stay), thereof cerebrospinal fluid (only once on day of surgery in patients with planned spinal anesthesia/combined spinal epidural analgesia in patients, only in Berlin).

A control group of ASA II/III- patients is collected for measuring the learning experience during the cognitive testings. The participants are matched on age, education, and gender to the study patients. The ASA II/III- control patients receive additionally MRI-scan (3 Tesla) at baseline, after 3 months and after 1 (Utrecht) and 2 years (Berlin).

To analyze scanner variability we additionally measure at maximum 20 subjects (Age ≥ 65 years, ASA I and II) from Utrecht in the MRI scanner (3-Tesla) in Berlin and vice versa.

A study group at maximum (n= 80) and is collected for measuring 7 Tesla MRI at two timepoints (Baseline and 90 days).The primary endponit of this substudy is gamma amino-butyric acid concentration in CNS after 3-months (measured by MRI). A retrospective comparison group (extracting 8000 intensive care unit patient data from the patient data management system during the BioCog study period in 2016) to analyse economic effects that are caused by the implementation of quality indicators in health care.

An interim-analysis is performed on the primary endpoint after 400 included patients.

The resulting (multivariate) expert system is expected: 1) to support clinical decision-making in patient care, e.g. to balance the individual POD/POCD risk against the expected overall clinical outcome of an (elective) surgical intervention, 2) to allow the design of more sophisticated and hypothesis-driven clinical studies and drug trials (translational research) in the future. The latter will be possible on the basis of biomarker-based sub-grouping of patients and a better understanding of relevant pathophysiological processes.

Furthermore, a state-of-the art clinical database and biobank will be created that does not yet exist worldwide. Both the expert system and the reference database/biobank will expand the leadership of the contributing academic institutions in this particular research area. In addition, the newly created biobank will become an integral part of the European Biobanking and Biomolecular Resources Research Infrastructure (BBMRI) which allows top address specific and hypothesis-driven research questions.

Most notably, the developed (multivariate) expert system also has the potential for commercialization. Possible customers are: 1) physicians and hospital departments being involved in pre-surgical decision making, 2) pharmaceutical industry intending to conduct biomarker-based drug trials in POD/POCD.

• Detailed Description: Not Provided
• Study Type: Observational
• Study Design: Observational Model: Cohort; Time Perspective: Prospective
• Target Follow-Up Duration: Not Provided

Biospecimen

Retention:   Samples With DNA

Description:

• Whole blood-/plasma (RNA-/DNA-Analysis)
• Cerebrospinal fluid (sequencing of candidate nicotinic receptor genes and genes for acetylcholine synthesis/-catabolism: CHRNA3, CHRNA4, CHRNA5, CHRNA7, CHRNB2, CHRNB4, ACHE, CHAT) (only in Berlin).

• Sampling Method: Non-Probability Sample
• Study Population: Surgical patients, 65 years or above (Berlin/Utrecht) ASA I and II patients, 65 years or above (Utrecht) ASA II and III patients, 65 years or above (Berlin/Utrecht)

Condition

• Postoperative Delirium (POD)
• Postoperative Cognitive Deficit (POCD)

• Intervention: Not Provided

Study Groups/Cohorts

• Surgical patients - 3 Tesla MRI

  A study group of at maximum n= 1200 is collected for measuring 3 Tesla MRI at two timepoints (Baseline and 90 days) in Berlin/Utrecht. They include surgical procedures within body cavity e.g. abdomen or thorax from departments of general surgery, urology, gynecology or thoracic surgery; orthopaedic operations (hip-, knee-, endoprosthesis or spine (including neurosurgical spine operations)); cardiac surgery and operation of extracranial/intracranial head and neck

  Data collection from study center Utrecht ist within one year after initial hospital stay. Data collection from study center Berlin is within two years after initial hospital stay.

• Patients ASA II/III - 3 Tesla MRI

  A control group of at maximum n= 300 ASA II/III- patients is collected for measuring the learning experience during the cognitive testings. They are matched on age, education, and gender to the study patients. The 104 ASA II/III- patients should receive additionally MRI-scan (3 Tesla) at baseline, after 3 months and after 1 year in Utrecht, after 3 months, after 1, 2 years in Berlin.

  Data collection from study center Utrecht ist within one year after initial hospital stay. Data collection from study center Berlin is within five years after initial hospital stay.

• Volunteers ASA I/II - 3 Tesla MRI
  To analyze scanner variability we additionally measure at maximum 20 subjects (Age ≥ 65 years) from Utrecht in the MRI scanner (3-Tesla) in Berlin and vice versa.
• Surgical patients - 7 Tesla MRI
  A study Group of at maximum n= 80 should be collected for measuring 7 Tesla MRI at two timepoints (Baseline and 90 days) in Berlin.

Publications *

• Ditzel FL, van Montfort SJT, Vernooij LM, Kant IMJ, Aarts E, Spies CD, Hendrikse J, Slooter AJC, van Dellen E; Biomarker Development for Postoperative Cognitive Impairment in the Elderly Consortium. Functional brain network and trail making test changes following major surgery and postoperative delirium: a prospective, multicentre, observational cohort study. Br J Anaesth. 2023 Feb;130(2):e281-e288. doi: 10.1016/j.bja.2022.07.054. Epub 2022 Oct 17.
• Bosancic Z, Spies CD, Muller A, Winterer G, Piper SK, Heinrich M; BioCog Consortium. Association of cholinesterase activities and POD in older adult abdominal surgical patients. BMC Anesthesiol. 2022 Sep 16;22(1):293. doi: 10.1186/s12871-022-01826-y.
• Windmann V, Dreier JP, Major S, Spies C, Lachmann G, Koch S. Increased Direct Current-Electroencephalography Shifts During Induction of Anesthesia in Elderly Patients Developing Postoperative Delirium. Front Aging Neurosci. 2022 Jun 28;14:921139. doi: 10.3389/fnagi.2022.921139. eCollection 2022.
• Fislage M, Feinkohl I, Pischon T, Spies CD, Borchers F, Winterer G, Zacharias N; BioCog Consortium. Presurgical Thalamus Volume in Postoperative Delirium: A Longitudinal Observational Cohort Study in Older Patients. Anesth Analg. 2022 Jul 1;135(1):136-142. doi: 10.1213/ANE.0000000000005987. Epub 2022 Jun 16.
• Heinrich M, Sieg M, Kruppa J, Nurnberg P, Schreier PH, Heilmann-Heimbach S, Hoffmann P, Nothen MM, Janke J, Pischon T, Slooter AJC, Winterer G, Spies CD. Association between genetic variants of the cholinergic system and postoperative delirium and cognitive dysfunction in elderly patients. BMC Med Genomics. 2021 Oct 21;14(1):248. doi: 10.1186/s12920-021-01071-1.
• Koch S, Windmann V, Chakravarty S, Kruppa J, Yurek F, Brown EN, Winterer G, Spies C; BioCog Study Group. Perioperative Electroencephalogram Spectral Dynamics Related to Postoperative Delirium in Older Patients. Anesth Analg. 2021 Dec 1;133(6):1598-1607. doi: 10.1213/ANE.0000000000005668.
• Lichtner G, Zacharias N, Spies CD, Feinkohl I, Winterer G, Pischon T, von Dincklage F; BioCog Consortium. Resting state brain network functional connectivity is not associated with inflammatory markers and blood cell counts in older adults. Clin Neurophysiol. 2021 Jul;132(7):1677-1686. doi: 10.1016/j.clinph.2021.03.042. Epub 2021 May 2.
• Heinrich M, Muller A, Cvijan A, Morgeli R, Kruppa J, Winterer G, Slooter AJC, Spies CD; BioCog Consortium. Preoperative Comparison of Three Anticholinergic Drug Scales in Older Adult Patients and Development of Postoperative Delirium: A Prospective Observational Study. Drugs Aging. 2021 Apr;38(4):347-354. doi: 10.1007/s40266-021-00839-5. Epub 2021 Mar 15.
• Kant IMJ, de Bresser J, van Montfort SJT, Mutsaerts HJMM, Witkamp TD, Buijsrogge M, Spies C, Hendrikse J, Slooter AJC. Preoperative brain MRI features and occurrence of postoperative delirium. J Psychosom Res. 2021 Jan;140:110301. doi: 10.1016/j.jpsychores.2020.110301. Epub 2020 Nov 16.
• Deffland M, Spies C, Weiss B, Keller N, Jenny M, Kruppa J, Balzer F. Effects of pain, sedation and delirium monitoring on clinical and economic outcome: A retrospective study. PLoS One. 2020 Sep 2;15(9):e0234801. doi: 10.1371/journal.pone.0234801. eCollection 2020.
• van Montfort SJT, van Dellen E, Wattel LL, Kant IMJ, Numan T, Stam CJ, Slooter AJC. Predisposition for delirium and EEG characteristics. Clin Neurophysiol. 2020 May;131(5):1051-1058. doi: 10.1016/j.clinph.2020.01.023. Epub 2020 Feb 21.
• Feinkohl I, Borchers F, Burkhardt S, Krampe H, Kraft A, Speidel S, Kant IMJ, van Montfort SJT, Aarts E, Kruppa J, Slooter A, Winterer G, Pischon T, Spies C. Stability of neuropsychological test performance in older adults serving as normative controls for a study on postoperative cognitive dysfunction. BMC Res Notes. 2020 Feb 4;13(1):55. doi: 10.1186/s13104-020-4919-3.
• Kant IMJ, Mutsaerts HJMM, van Montfort SJT, Jaarsma-Coes MG, Witkamp TD, Winterer G, Spies CD, Hendrikse J, Slooter AJC, de Bresser J; BioCog Consortium. The association between frailty and MRI features of cerebral small vessel disease. Sci Rep. 2019 Aug 5;9(1):11343. doi: 10.1038/s41598-019-47731-2.
• Windmann V, Spies C, Brown EN, Kishnan D, Lichtner G, Koch S; BioCog Study Group. Influence of midazolam premedication on intraoperative EEG signatures in elderly patients. Clin Neurophysiol. 2019 Sep;130(9):1673-1681. doi: 10.1016/j.clinph.2019.05.035. Epub 2019 Jul 10.
• Lachmann G, Kant I, Lammers F, Windmann V, Spies C, Speidel S, Borchers F, Hadzidiakos D, Hendrikse J, Winterer G, de Bresser J; BIOCOG Consortium. Cerebral microbleeds are not associated with postoperative delirium and postoperative cognitive dysfunction in older individuals. PLoS One. 2019 Jun 14;14(6):e0218411. doi: 10.1371/journal.pone.0218411. eCollection 2019.
• Feinkohl I, Janke J, Hadzidiakos D, Slooter A, Winterer G, Spies C, Pischon T. Associations of the metabolic syndrome and its components with cognitive impairment in older adults. BMC Geriatr. 2019 Mar 7;19(1):77. doi: 10.1186/s12877-019-1073-7.

Recruitment Information

• Recruitment Status: Terminated
• Actual Enrollment (submitted: September 23, 2019): 1054
• Original Estimated Enrollment (submitted: October 14, 2014): 1200
• Actual Study Completion Date: June 2019
• Actual Primary Completion Date: December 2017 (Final data collection date for primary outcome measure)

Eligibility Criteria

Study Group (Berlin/Utrecht):

Inclusion Criteria:

• Male and female patients aged ≥ 65 years, of European descent (Caucasian)
• Elective surgery with an expected operative time ≥ 60 minutes
• Ability to give informed consent after receiving spoken and written information of the study
• Eligibility for magnetic resonance Imaging

Exclusion Criteria:

• Mini-Mental-State-Examination ≤ 23 points
• Homelessness or other circumstances where the patient would not be reachable by phone or postal services during follow-up.
• Participation in another prospective interventional clinical study during participation in this clinical study during hospital stay
• Accommodation in an institution due to an official or judicial order
• Missing informed consent for saving and hand out pseudonymous data
• Neuropsychiatric morbidity, which limits the conduction of the neurocognitive testing
• Anacusis or Hypoacusis, which limits the conduction of the neurocognitive testing

Intraoperative clectroencephalography - examinations (Study Group Berlin):

Exclusion criteria:

• Neurological preconditions
• Proposed neurological surgery

Control Group (Berlin/Utrecht):

Inclusion criteria:

• Male and female patients aged ≥ 65 years, of European descent (Caucasian)
• ASA II and III patients
• No operation in the last half year before study inclusion
• Eligibility for magnetic resonance Imaging

Exclusion Criteria:

• Mini-Mental-State-Examination ≤ 23 Points
• Missing informed consent for saving and hand out pseudonymous data
• Neuropsychiatric morbidity, which limits the conduction of the neurocognitive testing
• Anacusis or Hypoacusis, which limits the conduction of the neurocognitive testing
• Taking psychothropic drugs (including sleep-inducing drug and benzodiazepine) on a regular basis and substances, which limit the conduction of the neurocognitive testing

Control Group (Utrecht) - Scannervariability:

Inclusion criteria:

• Male and female patients aged ≥ 65 years, of European descent (Caucasian)
• ASA I and II patients
• No operation in the last half year before study inclusion
• Eligibility for magnetic resonance Imaging

Study Group (Berlin) - 7 Tesla MRI:

Criteria as of the 3-Tesla- study group and additionally:

Exclusion criteria:

• absolute 7 - Tesla MRI-contraindications
• relative 7 - Tesla MRI-contraindications

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 65 Years and older (Older Adult)
• Accepts Healthy Volunteers: No
• Contacts: Contact information is only displayed when the study is recruiting subjects
• Listed Location Countries: Germany, Netherlands

Administrative Information

• NCT Number: NCT02265263
• Other Study ID Numbers: BioCog
• Has Data Monitoring Committee: No
• U.S. FDA-regulated Product: Not Provided
• IPD Sharing Statement: Not Provided
• Current Responsible Party: Claudia Spies, Charite University, Berlin, Germany
• Original Responsible Party: Same as current
• Current Study Sponsor: Charite University, Berlin, Germany
• Original Study Sponsor: Same as current
• Collaborators: European Union

Investigators

• Principal Investigator: Claudia Spies, MD Prof.; Department of Anesthesiology and Intensive Care Medicine, CVK/CCM, Charité - University Medicine Berlin
• Study Chair: Georg Winterer (BioCog Research Program Coordinator), MD, PhD; Department of Anesthesiology and Intensive Care Medicine, CVK/CCM, Charité - University Medicine Berlin

• PRS Account: Charite University, Berlin, Germany
• Verification Date: September 2019