check_circleStudy Completed

Tinea Versicolor

Bayer Identifier:

Trial_0125

ClinicalTrials.gov Identifier:

Not Available

EudraCT Number:

Not Available

EU CT Number:

Not Available
Study to test the efficacy and tolerance of BAY H 4502 1% solution in comparison with placebo and econazole solution in subjects with pityriasis versicolor

Trial purpose

Please see attached Study Results Summary below.

Key Participants Requirements

Sex

Both

Age

15 - 36 Years
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  • -

Trial summary

Enrollment Goal
60
Trial Dates
December 1979 - April 1980
Phase
Phase 2
Could I Receive a placebo
N/A
Products
Mycospor/Canesten Extra (Bifonazole, BAYH4502)
Accepts Healthy Volunteer
N/A

Trial design

Randomized, double blind control study to test the efficacy and tolerance of BAY H 4502 1% solution in comparison with placebo and econazole solution in subjects with pityriasis versicolor
Trial Type
Interventional
Intervention Type
N/A
Trial Purpose
N/A
Allocation
N/A
Blinding
N/A
Assignment
N/A
Trial Arms
N/A