Amphotericin B Suspension in Refractory Chronic Sinusitis

Status Completed

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00425620
Study type	Interventional
Source	Accentia Biopharmaceuticals
Contact
Status	Completed
Phase	Phase 3
Start date	December 2006
Completion date	October 2007

View Details

See also
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