drugset / Trial / NCT04607928
Pirfenidone Compared to Placebo in Post-COVID19 Pulmonary Fibrosis COVID-19
RandomizedParallel-groupTriple-blindPrevention
Summary
Study population: Patients with fibrotic lung sequelae after recovery from acute phase of severe COVID19 pneumonia Objectives: To evaluate the effect of pirfenidone administered for 24 weeks in patients who have pulmonary fibrotic changes after suffering severe COVID19 pneumonia, analysed by * % change in forced vital capacity (FVC) * % fibrosis in high resolution computed tomography (HRCT) of the lung
Timeline
- Start
- 2020-08-01
- Primary completion
- 2022-01-30
- Completion
- 2022-06-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Pirfenidone | Small molecule | 2403 mg | — |