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Completed Phase 2 Interventional Accepts healthy volunteers Results available

A Study to Evaluate Bleeding Patterns With Three Different Doses of DR-1031 Compared to Seasonale

ClinicalTrials.gov ID: NCT00394771

Public ClinicalTrials.gov record NCT00394771. 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 22, 2026, 5:02 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 Prospective, Multicenter, Double-Blinded, Randomized Study to Evaluate Bleeding Patterns in Women Using One of Three Different Doses of DR-1031 Oral Contraceptive Compared to Seasonale Oral Contraceptive Regimen

Study identification

NCT ID
NCT00394771
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Duramed Research
Industry
Enrollment
567 participants

Conditions and interventions

Interventions

  • DR-1031 Drug
  • Seasonale® Drug
  • Portia® 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
Sep 30, 2006
Primary completion
Feb 29, 2008
Completion
Feb 29, 2008
Last update posted
Jul 25, 2013

2006 – 2008

United States locations

U.S. sites
50
U.S. states
25
U.S. cities
48
Facility City State ZIP Site status
Duramed Investigational Site Huntsville Alabama 35801
Duramed Investigational Site Tucson Arizona 85741
Duramed Investigational Site Little Rock Arkansas 72205
Duramed Investigational Site San Diego California 92108
Duramed Investigational Site San Francisco California 94102
Duramed Investigational Site Santa Ana California 92705
Duramed Investigational Site Vista California 92083
Duramed Investigational Site Pueblo Colorado 81001
Duramed Investigational Site Stratford Connecticut 06615
Duramed Investigational Site DeLand Florida 32720
Duramed Investigational Site Jacksonville Florida 32207
Duramed Investigational Site Melbourne Florida 32935
Duramed Investigational Site Miami Florida 33186
Duramed Investigational Site Tampa Florida 33607
Duramed Investigational Site West Palm Beach Florida 33401
Duramed Investigational Site West Palm Beach Florida 33407
Duramed Investigational Site Alpharetta Georgia 30005
Duramed Investigational Site Douglasville Georgia 30134
Duramed Investigational Site Savannah Georgia 31406
Duramed Investigational Site Boise Idaho 83712
Duramed Investigational Site Meridian Idaho 83642
Duramed Investigational Site Fort Wayne Indiana 46825
Duramed Investigational Site Wichita Kansas 67205
Duramed Investigational Site Baton Rouge Louisiana 70808
Duramed Investigational Site Metairie Louisiana 70006
Duramed Investigational Site Shreveport Louisiana 71106
Duramed Investigational Site Riverdale Maryland 20737
Duramed Investigational Site Kansas City Missouri 64114
Duramed Investigational Site Las Vegas Nevada 89109
Duramed Investigational Site Las Vegas Nevada 89128
Duramed Investigational Site North Las Vegas Nevada 89030
Duramed Investigational Site Lebanon New Hampshire 03756
Duramed Investigational Site Cary North Carolina 27511
Duramed Investigational Site New Bern North Carolina 28562
Duramed Investigational Site Winston-Salem North Carolina 27103
Duramed Investigational Site Cleveland Ohio 44122
Duramed Investigational Site Mayfield Heights Ohio 44124
Duramed Investigational Site Eugene Oregon 97401
Duramed Investigational Site Medford Oregon 97504
Duramed Investigational Site Pittsburgh Pennsylvania 15206
Duramed Investigational Site Charleston South Carolina 29425
Duramed Investigational Site Columbia South Carolina 29201
Duramed Investigational Site Hilton Head Island South Carolina 29926
Duramed Investigational Site Jackson Tennessee 38305
Duramed Investigational Site Austin Texas 78737
Duramed Investigational Site Dallas Texas 75390
Duramed Investigational Site Houston Texas 77024
Duramed Investigational Site San Antonio Texas 78229
Duramed Investigational Site Salt Lake City Utah 84102
Duramed Investigational Site Williston Vermont 05495

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 NCT00394771, 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 Jul 25, 2013 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00394771 live on ClinicalTrials.gov.

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