Acute Phase Reactant in Non-COVID-19 Bacterial Pneumonia
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ClinicalTrials.gov Identifier: NCT05926089 |
Recruitment Status :
Completed
First Posted : July 3, 2023
Last Update Posted : July 14, 2023
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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 |
51 patients were included in our study, diagnosed as Non-COVID pneumonia
Inclusion criteria:
- PCR(polymerase chain reaction) negative for COVID.
- All patients of both sexes with pneumonia .
Exclusion criteria:
- Non pulmonary infections.
- Post surgery patients.
- Renal patients.
- hepatic patients.
- Cardiac patients.
- Recent pulmonary embolism.
Methodology in details:
All patients were subjected to:
-
Full history with emphasis on:
- Epidemiological features (age, gender).
- Risk factors (smoking, DM).
- Clinical presentation (cough, Fever and duration of illness).
- Clinical examination (local chest examination).
- Laboratory investigations: venous blood samples were taken to measure APR
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 |
- Diagnostic Test: Blood sampling
blood sampling to measure APR
- 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
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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 |
All patients( 51 patients diagnosed as non-COVID19 Pneumonia) were subjected to:
-
Full historywith emphasis on:
- Epidemiological features .
- Risk factors (smoking, DM).
- Clinical presentation (cough, Fever and duration of ilness).
- Clinical examination (local chest examination).
- Laboratory investigations: venous blood samples were taken for:• Complete blood picture, differential leucocytic count and platelets count, ESR ,CRP, d-dimer and ferritin
Inclusion Criteria:
- COVID-19 negative bacterial pneumonia
Exclusion Criteria:
- COVID-19 positive
- other non-pulmonary infections
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
Egypt | |
Kasr alainy school of medicine | |
Cairo, Egypt, 11562 |
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 |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Pneumonia Acute-Phase Reaction Respiratory Tract Infections Infections |
Lung Diseases Respiratory Tract Diseases Inflammation Pathologic Processes |