drugset / Trial / NCT04232449
Oral Corticosteroids for Post-infectious Cough in Adults
Phase 3
Terminated
32 enrolled
University Hospital, Basel, Switzerland
Swiss National Science Foundation · collab
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose of this study is to assess whether a 5-day treatment with orally administered prednisone provides patient-relevant benefits by improving the cough-related QoL of patients with post-infectious cough triggered by an Upper Respiratory Tract Infection (URTI) and seeking care in adult primary care practices. The study aims to describe an efficacy and safety profile for a 5-day prednisone treatment compared to a 5-day course of placebo.
Timeline
- Start
- 2020-11-06
- Primary completion
- 2024-04-30
- Completion
- 2024-04-30
Outcome
Outcome not reported
Stopped: “too few patients were included”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Prednisone | Other / unclassified | 40 mg | Oral |