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Completed Phase 3 Interventional Accepts healthy volunteers

Evaluate Safety and Efficacy of an OC Preparation vs Placebo for 6 Treatment Cycles in Women With Moderate Acne.

ClinicalTrials.gov ID: NCT00651469

Public ClinicalTrials.gov record NCT00651469. 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 Jun 26, 2026, 1:04 PM 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 Multicenter, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate Safety & Efficacy of Oral Contraceptive Prep., Containing Drospirenone 3 mg/Ethinyl Estradiol 20 Mcg for 6 Treatment Cycles in Women With Moderate Acne Vulgaris.

Study identification

NCT ID
NCT00651469
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bayer
Industry
Enrollment
534 participants

Conditions and interventions

Conditions

Interventions

  • YAZ (DRSP 3 mg/EE 0.02 mg, BAY86-5300) Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
14 Years to 45 Years
Sex
Female
Healthy volunteers
Accepts healthy volunteers

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

Study timeline

Start date
Dec 31, 2002
Primary completion
Not listed
Completion
Jun 30, 2004
Last update posted
Dec 29, 2014

2003 – 2004

United States locations

U.S. sites
27
U.S. states
18
U.S. cities
26
Facility City State ZIP Site status
Not listed Birmingham Alabama 35209
Not listed Huntsville Alabama 35801
Not listed Mesa Arizona 85201
Not listed Los Angeles California 90010
Not listed San Diego California 92108
Not listed Washington D.C. District of Columbia 20010-2975
Not listed Miami Florida 33175
Not listed St. Petersburg Florida 33702
Not listed Tampa Florida 33607
Not listed Boise Idaho 83704
Not listed Chicago Illinois 60631
Not listed Indianapolis Indiana 46250
Not listed New Orleans Louisiana 70115
Not listed Wellesley Massachusetts 02481
Not listed Kansas City Missouri 64114
Not listed Albuquerque New Mexico 87106
Not listed Winston-Salem North Carolina 27103
Not listed Winston-Salem North Carolina 27157
Not listed Cincinnati Ohio 45230
Not listed Hershey Pennsylvania 17033-0850
Not listed Philadelphia Pennsylvania 19114
Not listed Warwick Rhode Island 02886
Not listed Austin Texas 78759
Not listed Dallas Texas 75230
Not listed Houston Texas 77024
Not listed San Antonio Texas 78229
Not listed Tacoma Washington 98405

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 NCT00651469, 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 Dec 29, 2014 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00651469 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →