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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00913185
Other study ID # 1021
Secondary ID
Status Completed
Phase Phase 4
First received March 1, 2007
Last updated June 23, 2014
Start date December 2006
Est. completion date February 2008

Study information

Verified date June 2014
Source MedDerm Associates
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare the effectiveness of two over the counter acne products in subjects with moderate severity acne vulgaris. The two products being compared in this study are Acne Free "Severe Acne Line" manufactured by University Medical Products, and Proactiv® manufactured by Guthy-Renker.


Description:

You will receive a study drug for the 8 week study. No subject will be given a placebo (an inactive substance) during treatment.The study drugs (over the counter acne medications) have been previously tested and their safe use has been established. However, not all risks or side effects are known. In rare cases of allergy, side effects may be life threatening.The most common side effects of this study drug are:

1. Dry skin

2. Peeling skin

3. Red skin

4. Burning or tingling (temporary)


Other known NCT identifiers
  • NCT00419523

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Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Acne Free, Proactiv


Locations

Country Name City State
United States MedDerm Associates San Diego California

Sponsors (1)

Lead Sponsor Collaborator
MedDerm Associates

Country where clinical trial is conducted

United States, 

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