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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 Oct 23, 2026, 9:05 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

Brief summary

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

This study will evaluate the superiority of ulipristal acetate versus placebo for the treatment of abnormal uterine bleeding associated with uterine fibroids

Study identification

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

Conditions and interventions

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 31, 2014 (Actual)
Primary completion
Mar 29, 2016 (Actual)
Completion
Mar 29, 2016 (Actual)
Last update posted
Apr 30, 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 30, 2019 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02147197 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →