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Completed Not applicable Interventional Accepts healthy volunteers Results available

Laparoscopic Radiofrequency Ablation (RFA) of Symptomatic Uterine Fibroids

ClinicalTrials.gov ID: NCT00874029

Public ClinicalTrials.gov record NCT00874029. 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, 6:07 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 Halt System for Laparoscopic Treatment of Symptomatic Uterine Fibroids With Radiofrequency Ablation

Study identification

NCT ID
NCT00874029
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Acessa Health, Inc.
Industry
Enrollment
137 participants

Conditions and interventions

Interventions

  • Halt Procedure Device

Device

Eligibility (public fields only)

Age range
25 Years and older
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
Feb 28, 2009
Primary completion
Dec 31, 2011
Completion
Feb 28, 2014
Last update posted
Jul 2, 2014

2009 – 2014

United States locations

U.S. sites
9
U.S. states
7
U.S. cities
9
Facility City State ZIP Site status
Women's Health Research Phoenix Arizona 85015
USC Medical Center Los Angeles California 90033
Pasadena Premier Women's Health Pasadena California 91145
Reproductive Science Center San Ramon California 94583
Wayne State University Detroit Michigan 48034
St. Luke's Hospital Chesterfield Missouri 63017
Athena Gynecology Medical Group Reno Nevada 89509
Montefiore Medical Center The Bronx New York 10461
Magee-Women's Hospital Pittsburgh Pennsylvania 15213

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00874029, 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 2, 2014 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00874029 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →