Trials / Completed
CompletedNCT01433107
Efficacy and Safety of Terbinafine Film Forming Solution in Patients With Tinea Pedis
A Randomized, Double-blind, Placebo-controlled, Multicenter, Parallel Group Study of the Efficacy and Safety of Terbinafine Film Forming Solution, 1% (as Hydrochloride), in Patients With Tinea Pedis
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 290 (actual)
- Sponsor
- Novartis · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study will compare the efficacy and safety of a single dose of terbinafine film forming solution 1% with a single dose of placebo film forming solution in the treatment of tinea pedis.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Terbinafine | 1% single application |
| DRUG | Terbinafine Placebo | single application |
Timeline
- Start date
- 2011-08-01
- Primary completion
- 2012-02-01
- Completion
- 2012-02-01
- First posted
- 2011-09-13
- Last updated
- 2013-12-27
- Results posted
- 2013-12-27
Locations
6 sites across 1 country: China
Source: ClinicalTrials.gov record NCT01433107. Inclusion in this directory is not an endorsement.