drugset / Trial / NCT04140214
Randomised Open Label Trial of Hypertonic Saline and Carbocisteine in Bronchiectasis (CLEAR)
Phase 3
Completed
288 enrolled
Belfast Health and Social Care Trust
Queen's University, Belfast · collab
RandomizedFactorialOpen-labelTreatment
Summary
Patients with bronchiectasis (BE) suffer from a persistent cough, daily sputum expectoration, recurrent chest infections, and a poor health-related quality of life. Current guidelines for the management of BE highlight the lack of evidence to recommend mucoactive agents, such as hypertonic saline (HTS) and carbocisteine, to aid sputum-removal as part of standard care. The investigators hypothesise that mucoactive agents (HTS or cabocisteine, or a combination of both) are effective in reducing exacerbations over a 52-week period, compared to usual care.
Timeline
- Start
- 2018-06-27
- Primary completion
- 2024-09-30
- Completion
- 2024-12-18
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Carbocysteine | Unknown | 750 mg | — |
| Subject | Hypertonic saline | Unknown | 4 ml | Inhaled |
| Subject | Hypertonic saline | Unknown | 6 % | Inhaled |