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Completed Phase 3 Interventional Accepts healthy volunteers

Efficacy and Safety Study of an Oral Contraceptive in Healthy Females

ClinicalTrials.gov ID: NCT00206583

Public ClinicalTrials.gov record NCT00206583. 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 Sep 5, 2026, 7:44 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 Multicenter, Open-label Uncontrolled Study to Investigate the Efficacy and Safety of a 4-phasic Oral Contraceptive SH T0065 in a 28-day Regimen for 13 Cycles in Healthy Female Subjects

Brief summary

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

The purpose of this study is to determine whether the study drug is safe and effective in the prevention of pregnancies in a large group of volunteers.

Study identification

NCT ID
NCT00206583
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bayer
Industry
Enrollment
499 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 35 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
Feb 28, 2005
Primary completion
May 31, 2007
Completion
Jun 30, 2007
Last update posted
Sep 30, 2014

2005 – 2007

United States locations

U.S. sites
20
U.S. states
11
U.S. cities
19
Facility City State ZIP Site status
Women and Children's Hospital, Los Angeles Los Angeles California 90033
Lifespan Research Palo Alto California 94301
Genesis Center for Clinical Research San Diego California 92103
Medical Center for Clinical Research San Diego California 92108
Harbor - UCLA Medical Center Torrance California 90509
Clinical Trial Center of Colorado Castle Rock Colorado 80108
New Age Medical Research Corp. Miami Florida 33186
Visions Clinical Research Palm Springs Florida 33461
Insignia Care for Women, P.A. Tampa Florida 33607
Comprehensive Clinical Trials West Palm Beach Florida 33409
Physicians Research Group Indianapolis Indiana 46250
Johns Hopkins Bayview Medical Center Baltimore Maryland 21224
Women's Clinic of Lincoln, PC Lincoln Nebraska 68510
Women's Care Source Morristown New Jersey 07960
OB/GYN Health Center Medford Oregon 97504
Oregon Health and Science University Portland Oregon 97239
Clinical Research of Philadelphia, LLC Philadelphia Pennsylvania 19114
University of Pittsburgh Medical Center Health System Pittsburgh Pennsylvania 15213-2582
Eastern Virginia Medical School Norfolk Virginia 23507
Seattle Women's: Health, Research, Gynecology Seattle Washington 98105

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 9 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00206583, 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 Sep 30, 2014 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00206583 live on ClinicalTrials.gov.

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