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Completed Phase 4 Interventional Results available

A Study of Different Use Regimens Using Two Acne Treatments

ClinicalTrials.gov ID: NCT00907257

Public ClinicalTrials.gov record NCT00907257. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 3:26 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Clinical Assessment of the Use of RETIN-A MICRO (Tretinoin Gel) Microsphere, 0.04% in a Pump Dispenser and a 5% Benzoyl Peroxide Wash Used in the Morning Compared to the Use of RETIN-A MICRO 0.04% Pump Nightly and a 5% Benzoyl Peroxide Wash in the Morning For the Treatment of Facial Acne Vulgaris

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A study to determine if using 2 acne products in the morning is as safe and efficacious as using one product in the morning and one product in the evening.

Study identification

NCT ID
NCT00907257
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Bausch Health Americas, Inc.
Industry
Enrollment
247 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 2009 (Type not available)
Primary completion
Sep 2009 (Actual)
Completion
Sep 2009 (Actual)
Last update posted
Feb 15, 2012

2009

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Skin Care Research, Inc. Boca Raton Florida 33486 —
International Dermatology Research, Inc. Miami Florida 33144 —
Gwinnett Clinical Research Snellville Georgia 30078 —
Derm Research, PLLC Louisville Kentucky 40217 —
Minnesota Clinical Study Center Fridley Minnesota 55432 —
Academic Dermatology Associates Albuquerque New Mexico 87106 —
DermResearch Center of New York Stony Brook New York 11790 —
Dermatology Research Associates Cincinnatti Ohio 45230 —
Yardley Dermatology Associates Yardley Pennsylvania 19067 —
DermResearch, Inc. Austin Texas 78759 —
Education & Research Foundation, Inc. Lynchburg Virginia 24501 —
Virginia Clinical Research, Inc. Norfolk Virginia 23507 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00907257, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 15, 2012 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00907257 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →