CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 61 enrolled
Drug / intervention
draw bloodother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04369820
NCT04369820N/ACompleted

C5a Receptor Expression in Circulating Myeloid Cells in ARDS Secondary to COVID-19

Assistance Publique Hopitaux De Marseille·interventional·Posted Apr 30, 2020·Updated Aug 14, 2023

In Brief

A clinical study evaluating draw blood for COVID-19. Completed, enrolled 61 participants across 1 site.

Detailed Summary

The pathophysiology of ARDS is linked to an uncontrolled inflammatory response at the level of alveolo-capillary membrane, mediated by neutrophils and mononuclear cells. The complement system and anaphylatoxin C5a have shown central role in the recruitment of these pro-inflammatory cells and more broadly in the genesis of cytokinic storm syndrome. C5a acts via receptors C5aR and C5L2. This is a preliminary study aimed at studying the expression of the C5a receptor on myeloid cells in peripheral blood of patients with ARDS secondary to COVID-19. This study has of primary objective to show there is an overexpression of the C5a receptor in patients with ARDS secondary to COVID-19 compared to control patients (patients with COVID-19 without respiratory distress and healthy volunteers). The medium-term objective is to develop a clinical trial to test the effectiveness of anti-C5aR antibody in this condition.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCOVID-19
CountriesFrance
CollaboratorsInnate Pharma

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedApr 30, 2020
Enrollment StartMar 31, 2020
Primary CompletionSep 30, 2020
Study CompletionAug 9, 2023
TodayJul 2, 2026
Enrollment to primary: 6 monthsPosted 6.2 years ago

Interventions

draw bloodother

40 mL blood sample will be taken within the first three days of hospitalization, a second sample will be taken between the 5th and 10th day of hospitalization and a third sample will be taken on the 10th day of hospitalization or the day of discharge if earlier.