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Relationship Between Intracranial Blood Flow and Peripheral Perfusion in Patients With Craniocerebral Injury

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT06016751
Recruitment Status : Completed
First Posted : August 30, 2023
Last Update Posted : August 30, 2023
Sponsor:
Information provided by (Responsible Party):
Peking Union Medical College Hospital

Brief Summary:
Neurocritical care is a major branch in the field of critical care medicine, and more than 50% of the neurocritical care patients in the Tibet Autonomous Region People's Hospital (TARPH) are in neurocritical care, of which cranial damage accounts for about 30%, and paroxysmal sympathetic hyperexcitability syndrome (PSH) after traumatic brain injury(TBI)is a common complication, which affects the cardiorespiratory and cerebral functions to varying degrees, and optimizing the cerebral perfusion and oxygenation supply is the key point in the treatment of TIB, and the maintenance of the cerebral homeostasis and the functional homeostasis is currently an international hotspot for treatment. Maintaining cerebral homeostasis and body function homeostasis is an international hotspot in the treatment of TIB. This study intends to elaborate on the relationship between PSH and Intracranial blood flow in patients with TBI, as well as the effect of anti-stress treatment on Intracranial blood flow. Implementation Patients with brain injury admitted to our department from January 2021 to January 2022 were included. Non-invasive transcranial Doppler ultrasound was applied to measure cerebral blood flow, non-invasive local cerebral oxygen saturation monitor to measure local cerebral oxygen saturation, and an electroencephalography bispectrometer to measure BIS score to quantify the depth of sedation during the experimental process. Bedside ultrasound monitored the right heart function and lung water status, and the data of each monitoring index were monitored and recorded throughout the whole process, and the relationship between concomitant PSH and Intracranial blood flow in TBI patients was found according to the statistical analysis. Ultimately, to achieve the control of TBI complications and improve patient rescue. To expect to achieve the purpose of improving the prognosis of TBI patients.

Condition or disease
Brain-injury Intracranial; Blood Vessel, Injury

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Study Type : Observational
Actual Enrollment : 30 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Relationship Between Intracranial Blood Flow and Peripheral Perfusion in Patients With Craniocerebral Injury Assessed by Doppler Ultrasound and Prognostic Assessment
Actual Study Start Date : January 1, 2021
Actual Primary Completion Date : January 1, 2022
Actual Study Completion Date : January 1, 2022

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Head Injuries

Group/Cohort
cranial damage
Our study was a prospective observational study which included only a group of patients who were diagnosed with acute craniocerebral injury.



Primary Outcome Measures :
  1. intracranial blood flow [ Time Frame: Day 1,Day 3,Day 5 ]
    Mean intracranial middle cerebral artery blood flow velocity and pulsatility index measured using ultrasound Doppler in enrolled patients.

  2. Paroxysmal sympathetic excitation [ Time Frame: Day 1,Day 3,Day 5 ]
    Use of the Paroxysmal Sympathetic Nerve Score to assess paroxysmal sympathoexcitatory performance in patients.



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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Definite craniocerebral injury, surgically treated and transferred to ICU.
Criteria

Inclusion Criteria:

  • Craniocerebral injury patients;
  • The middle cerebral artery blood flow spectrum can be clearly displayed with a bedside TCD;

Exclusion Criteria:

  • Age Under 18 years;
  • history of cardiovascular disease such as coronary artery disease, heart failure, or atrial fibrillation;
  • presence of severe valvular disease or ejection fraction (EF) <30%;
  • chronic lung disease;
  • chronic liver failure or renal insufficiency;
  • persons with co-morbidities of malignant neoplasms;
  • persons who had co-morbidities with acute and chronic infectious diseases prior to craniocerebral injuries;
  • women who were pregnant and breastfeeding;
  • history of psychiatric disorders;
  • history of drug abuse or alcohol misuse;
  • history of β-blockers;
  • co-morbidities with spinal cord injuries; and persons who had died or been discharged from hospital within 1 week of hospitalization or who had not been able to obtain a clear image with ultrasonography.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT06016751


Locations
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China, Beijing
Wei Du
Beijing, Beijing, China
Sponsors and Collaborators
Peking Union Medical College Hospital
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Responsible Party: Peking Union Medical College Hospital
ClinicalTrials.gov Identifier: NCT06016751    
Other Study ID Numbers: YLong
First Posted: August 30, 2023    Key Record Dates
Last Update Posted: August 30, 2023
Last Verified: August 2023

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Brain Injuries
Craniocerebral Trauma
Wounds and Injuries
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Trauma, Nervous System