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Completed Phase 3 Interventional Results available

A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas

ClinicalTrials.gov ID: NCT02147197

Public ClinicalTrials.gov record NCT02147197. 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, 4:28 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 Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas

Study identification

NCT ID
NCT02147197
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Allergan
Industry
Enrollment
157 participants

Conditions and interventions

Interventions

  • Ulipristal acetate (UPA) Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 50 Years
Sex
Female
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
Mar 30, 2014
Primary completion
Mar 28, 2016
Completion
Mar 28, 2016
Last update posted
Apr 29, 2019

2014 – 2016

United States locations

U.S. sites
28
U.S. states
18
U.S. cities
26
Facility City State ZIP Site status
Watson Investigational Site 125 Tucson Arizona 85710
Watson Investigational Site 102 San Diego California 92103
Watson Investigational Site 112 Denver Colorado 80209
Watson Investigational Site 115 Lakewood Colorado 80228
Watson Investigational Site 116 Milford Connecticut 06460
Watson Investigational Site 114 Washington D.C. District of Columbia 20036
Watson Investigational Site 106 Clearwater Florida 33765
Watson Investigational Site 122 Lake Worth Florida 33461
Watson Investigational Site 130 Miami Florida 33176
Watson Investigational Site 105 New Port Richey Florida 34652
Watson Investigational Site 104 Orlando Florida 32806
Watson Investigational Site 120 Orlando Florida 32806
Watson Investigational Site 103 Atlanta Georgia 30338
Watson Investigational Site 123 Atlanta Georgia 30342
Watson Investigational Site 111 Augusta Georgia 30912
Watson Investigational Site 124 Idaho Falls Idaho 83404
Watson Investigational Site 131 Brownsburg Indiana 46112
Watson Investigational Site 129 Shawnee Mission Kansas 66218
Watson Investigational Site 132 Metairie Louisiana 70006
Watson Investigational Site 110 Norfolk Nebraska 68701
Watson Investigational Site 113 Albuquerque New Mexico 87109
Watson Investigational Site 121 Raleigh North Carolina 27607
Watson Investigational Site 109 Winston-Salem North Carolina 27103
Watson Investigational Site 107 Columbus Ohio 43231
Watson Investigational Site 119 Jenkintown Pennsylvania 19046
Watson Investigational Site 108 Myrtle Beach South Carolina 29572
Watson Investigational Site 101 Chattanooga Tennessee 37404
Watson Investigational Site 126 Memphis Tennessee 38119

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 NCT02147197, 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 29, 2019 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02147197 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →