The classic website will no longer be available as of June 25, 2024. Please use the modernized ClinicalTrials.gov.
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Acute Phase Reactant in Non-COVID-19 Bacterial Pneumonia

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: NCT05926089
Recruitment Status : Completed
First Posted : July 3, 2023
Last Update Posted : July 14, 2023
Sponsor:
Information provided by (Responsible Party):
Eman Kamal Ibrahim Hassan, Cairo University

Brief Summary:

This study is a cross-sectional study, was conducted at Chest department of Kasr Al-ainy Hospital, Cairo university during the period between October 2020 and April 2021.

The aim of the work was to evaluate levels of acute phase reactants(APR) in Non-COVID-19 bacterial pneumonia, and to correlate between levels of APR and the disease severity.


Condition or disease Intervention/treatment
Pneumonia Acute-Phase Reaction Diagnostic Test: Blood sampling

Detailed Description:

51 patients were included in our study, diagnosed as Non-COVID pneumonia

Inclusion criteria:

  1. PCR(polymerase chain reaction) negative for COVID.
  2. All patients of both sexes with pneumonia .

Exclusion criteria:

  1. Non pulmonary infections.
  2. Post surgery patients.
  3. Renal patients.
  4. hepatic patients.
  5. Cardiac patients.
  6. Recent pulmonary embolism.

Methodology in details:

All patients were subjected to:

  1. Full history with emphasis on:

    • Epidemiological features (age, gender).
    • Risk factors (smoking, DM).
    • Clinical presentation (cough, Fever and duration of illness).
  2. Clinical examination (local chest examination).
  3. Laboratory investigations: venous blood samples were taken to measure APR

Layout table for study information
Study Type : Observational
Actual Enrollment : 51 participants
Observational Model: Case-Only
Time Perspective: Cross-Sectional
Official Title: Acute Phase Reactant in Non-COVID-19 Community Acquired Pneumonia
Actual Study Start Date : October 1, 2020
Actual Primary Completion Date : April 30, 2021
Actual Study Completion Date : May 30, 2021



Intervention Details:
  • Diagnostic Test: Blood sampling
    blood sampling to measure APR


Primary Outcome Measures :
  1. measurement of APR levels in non-Covid-19 pneumonia [ Time Frame: 6 months ]
    assessment of the level of APR and its relation to disease severity


Biospecimen Retention:   Samples Without DNA
• Complete blood picture, differential leucocytic count and platelets count: Done by The newly developed automated hematology analyzer (Sysmex, Kobe, Japan) enumerates and classifies blood cells by a combination of direct current detection and flow cytometry. (Daves et al., 2015).


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 75 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

All patients( 51 patients diagnosed as non-COVID19 Pneumonia) were subjected to:

  1. Full historywith emphasis on:

    • Epidemiological features .
    • Risk factors (smoking, DM).
    • Clinical presentation (cough, Fever and duration of ilness).
  2. Clinical examination (local chest examination).
  3. Laboratory investigations: venous blood samples were taken for:• Complete blood picture, differential leucocytic count and platelets count, ESR ,CRP, d-dimer and ferritin
Criteria

Inclusion Criteria:

  • COVID-19 negative bacterial pneumonia

Exclusion Criteria:

  • COVID-19 positive
  • other non-pulmonary infections

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): NCT05926089


Locations
Layout table for location information
Egypt
Kasr alainy school of medicine
Cairo, Egypt, 11562
Sponsors and Collaborators
Cairo University
Layout table for additonal information
Responsible Party: Eman Kamal Ibrahim Hassan, Assistant Professor of pulmonology, Cairo University
ClinicalTrials.gov Identifier: NCT05926089    
Other Study ID Numbers: MS-358-2020
First Posted: July 3, 2023    Key Record Dates
Last Update Posted: July 14, 2023
Last Verified: July 2023
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
Layout table for MeSH terms
Pneumonia
Acute-Phase Reaction
Respiratory Tract Infections
Infections
Lung Diseases
Respiratory Tract Diseases
Inflammation
Pathologic Processes