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Not listed Phase 3 Interventional

Safety & Effectiveness Study of AEGEA Vapor System to Treat Excessive Uterine Bleeding

ClinicalTrials.gov ID: NCT01979861

Public ClinicalTrials.gov record NCT01979861. 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 25, 2026, 10:12 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 Prospective, Multicenter, Clinical Trial to Evaluate the Safety and Effectiveness of the AEGEA Vapor System for the Treatment of Excessive Uterine Bleeding

Brief summary

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

The purpose of this study is to determine if the AEGEA Vapor System for endometrial ablation is safe and effective for reducing menstrual blood loss in women with excessive uterine bleeding (menorrhagia)

Study identification

NCT ID
NCT01979861
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Aegea Medical, Inc.
Industry
Enrollment
230 participants

Conditions and interventions

Conditions

Interventions

Device

Eligibility (public fields only)

Age range
30 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
Feb 2014 (Type not available)
Primary completion
Jun 2016 (Actual)
Completion
Jun 2018 (Estimated)
Last update posted
Jul 12, 2016

2014 – 2018

United States locations

U.S. sites
12
U.S. states
11
U.S. cities
12
Facility City State ZIP Site status
Center for Fertility and Women's Health New Britain Connecticut 06051 —
Clinical Associates of Orlando, LLC Orlando Florida 32801 —
Visions Clinical Research Wellington Florida 33414 —
Rosemark WomenCares Specialists Idaho Falls Idaho 83404 —
The Advanced Gynecologic Surgery Institute Naperville Illinois 60173 —
Basinksi, LLC Newburgh Indiana 47630 —
Minnesota Gynecology & Surgery Edina Minnesota 55435 —
Mercy Hospital St Louis Missouri 63141 —
Montefiore Medical Center The Bronx New York 10467 —
Carolina Women's Research and Wellness Center/OB-GYN Durham North Carolina 27713 —
Chattanooga Medical Research, LLC Chattanooga Tennessee 37404 —
Baylor All Saints Fort Worth Texas 76104 —

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 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01979861, 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 12, 2016 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01979861 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →