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Completed Not applicable Interventional Results available

Sonography Guided Transcervical Ablation of Uterine Fibroids

ClinicalTrials.gov ID: NCT02228174

Public ClinicalTrials.gov record NCT02228174. 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 21, 2026, 6:05 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

Evaluation of the Gynesonics System for Transcervical Treatment of Symptomatic Uterine Fibroids With Radiofrequency Ablation Under Integrated Intrauterine Sonography Guidance

Study identification

NCT ID
NCT02228174
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Gynesonics
Industry
Enrollment
147 participants

Conditions and interventions

Conditions

Interventions

  • Intrauterine Ultrasound-Guided Radiofreq. Ablation System Device

Device

Eligibility (public fields only)

Age range
25 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
Sep 30, 2014
Primary completion
Oct 17, 2017
Completion
Oct 31, 2019
Last update posted
Feb 10, 2020

2014 – 2019

United States locations

U.S. sites
22
U.S. states
19
U.S. cities
22
Facility City State ZIP Site status
Kelly H. Roy M.D. P.C. Phoenix Arizona 85006
Advanced Women's Health Institute Denver Colorado 80246
Christiana Care Health Services, Inc. Newark Delaware 19718
George Washington University Hospital Washington D.C. District of Columbia 20037
KO Clinical Research, LLC Fort Lauderdale Florida 33316
Visions Clinical Research Wellington Florida 33414
The Advanced Gynecologic Surgery Institute - Charles E. Miller, MD & Associates Naperville Illinois 60540
University of Maryland Medical Center Baltimore Maryland 21201
Wayne State University Detroit Michigan 48201
University of Mississippi Medical Center Jackson Mississippi 39216
Mercy Clinic, Minimally Invasive Gynecology St Louis Missouri 63141
Cooper University Hospital Camden New Jersey 08103
Basque Women's Care Albuquerque New Mexico 87109
Montefiore Medical Center New York New York 10467
Carolina Women's Research and Wellness Center Durham North Carolina 27713
Drexel University Philadelphia Pennsylvania 19104
Magee Women's Hospital Pittsburgh Pennsylvania 15213
Greenville Health System Greenville South Carolina 29605
Baylor Research Institute Fort Worth Texas 76104
Willowbend Health and Wellness Associates Frisco Texas 75035
Eastern Virginia Medical School Norfolk Virginia 23507
Virginia Mason Medical Center Seattle Washington 98101

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02228174, 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 Feb 10, 2020 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02228174 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →