drugset / Trial / NCT00425620
Amphotericin B Suspension in Refractory Chronic Sinusitis
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The primary objective of the study is to evaluate the safety and efficacy of Amphotericin B suspension versus placebo in the complete resolution of key chronic sinusitis symptoms during 16 weeks of treatment in patients with refractory, postsurgical CS.
Timeline
- Start
- 2006-12
- Primary completion
- —
- Completion
- 2007-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Amphotericin B | Unknown | — | Intranasal |