drugset / Trial / NCT04744090

Roflumilast as add-on Therapy in Early Cases of ARDS

NCT04744090

Phase 2 Completed 76 enrolled Cairo University
RandomizedParallel-groupSingle-blindTreatment

Summary

* Mild cases of ARDS will be included in a two-arm protocol, to receive 500 mcg of roflumilast daily up to 28 days (FDA approved dose for COPD) plus standard of care versus standard of care alone. * Approximately 76 hospitalized patients with ARDS will be enrolled in this study. * Eligible patients will be randomized at ratio of (1:1) to receive either roflumilast plus standard of care or standard of care alone.

Timeline

Start
2021-03-21
Primary completion
2021-12-30
Completion
2022-01-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Roflumilast Small molecule 500 ug