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NCT06022198

Bronchoalveolar Lavage in Recovered From COVID-19 Pneumonia

Completed NA Last updated 1 September 2023
What this trial tests

NA trial testing Bronchoalveolar Lavage in Bronchoalveolar Lavage in 50 participants. Completed in 1 January 2023.

Timeline
1 January 2021
Primary endpoint
1 January 2022
1 January 2023

Quick facts

Lead sponsorMohamed Abd Elmoniem Mohamed
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment50
Start date1 January 2021
Primary completion1 January 2022
Estimated completion1 January 2023
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Mohamed Abd Elmoniem Mohamed

Who can join

18 and older, any sex, with Bronchoalveolar Lavage. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Coronaviruses such as SARS-CoV2, MERS-CoV, and SARS-CoV can cause significant morbidity and mortality in infected persons. Lung is the most common site of infection for these viruses, which may manifest as acute respiratory distress syndrome and mortality. Pulmonary involvement is also responsible for the high viral transmission The aim of this study is to evaluate BAL in post-acute COVID-19 patients for:Cytological and cellular patterns. Microbial analysis for possibility of presence of bacterial, mycobacerial or fungal co-infection.PCR for corona virus

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of Bronchoalveolar Lavage

Trials testing the same drug.

Other recruiting trials for Bronchoalveolar Lavage

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06022198.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing