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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Study of Safety and Efficacy of an Oral Contraceptive

ClinicalTrials.gov ID: NCT00932321

Public ClinicalTrials.gov record NCT00932321. 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 Jul 23, 2026, 4:17 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

Open Label, Randomized, Comparator-Controlled Study of the Contraceptive Efficacy of Norethindrone Acetate (NA) and Ethinyl Estradiol (EE)

Study identification

NCT ID
NCT00932321
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Warner Chilcott
Industry
Enrollment
938 participants

Conditions and interventions

Interventions

  • Norethindrone Acetate/Ethinyl Estradiol 24 Days Drug
  • Norethindrone Acetate /Ethinyl Estradiol 21 Days Drug

Drug

Eligibility (public fields only)

Age range
18 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, 2003
Primary completion
Oct 31, 2004
Completion
Oct 31, 2004
Last update posted
Apr 21, 2013

2004

United States locations

U.S. sites
34
U.S. states
14
U.S. cities
31
Facility City State ZIP Site status
Warner Chilcott Investigational Site Birmingham Alabama 35233
Warner Chilcott Investigational Site Phoenix Arizona 85014
Warner Chilcott Investigational Site Phoenix Arizona 85031
Warner Chilcott Investigational Site Chico California 95929
Warner Chilcott Investigational Site Los Angeles California 90033
Warner Chilcott Investigational Site San Diego California 92103
Warner Chilcott Investigational Site San Diego California 92108
Warner Chilcott Investigational Site Denver Colorado 80202
Warner Chilcott Investigational Site Boynton Beach Florida 33437
Warner Chilcott Investigational Site Jacksonville Florida 32207
Warner Chilcott Investigational Site Miami Florida 33186
Warner Chilcott Investigational Site Palm Harbor Florida 34684
Warner Chilcott Investigational Site Venice Florida 34285
Warner Chilcott Investigational Site West Palm Beach Florida 33409
Warner Chilcott Investigational Site Decatur Georgia 30033
Warner Chilcott Investigational Site Decatur Georgia 30034
Warner Chilcott Investigational Site Powder Springs Georgia 30127
Warner Chilcott Investigational Site Roswell Georgia 30075
Warner Chilcott Investigational Site Savannah Georgia 31405
Warner Chilcott Investigational Site Louisville Kentucky 40202
Warner Chilcott Investigational Site Kansas City Missouri 64112
Warner Chilcott Investigational Site St Louis Missouri 63117
Warner Chilcott Investigational Site New Bern North Carolina 28562
Warner Chilcott Investigational Site Winston-Salem North Carolina 27103
Warner Chilcott Investigational Site Allentown Pennsylvania 18104
Warner Chilcott Investigational Site Philadelphia Pennsylvania 19114
Warner Chilcott Investigational Site Pittsburgh Pennsylvania 15206
Warner Chilcott Investigational Site Charleston South Carolina 29425
Warner Chilcott Investigational Site Greenville South Carolina 29605
Warner Chilcott Investigational Site Sandy City Utah 84070
Warner Chilcott Investigational Site Norfolk Virginia 23507
Warner Chilcott Investigational Site Richmond Virginia 23233
Warner Chilcott Investigational Site Virginia Beach Virginia 23456
Warner Chilcott Investigational Site 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00932321, 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 Apr 21, 2013 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00932321 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →