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Completed Not applicable Interventional Results available

Minerva Pivotal Study to Evaluate Safety and Efficacy of the Aurora Endometrial Ablation System Compared to Hysteroscopic Rollerball Ablation

ClinicalTrials.gov ID: NCT01569763

Public ClinicalTrials.gov record NCT01569763. 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, 2:45 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

Minerva Pivotal Study

Study identification

NCT ID
NCT01569763
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Minerva Surgical, Inc.
Industry
Enrollment
153 participants

Conditions and interventions

Conditions

Interventions

  • Aurora Endometrial Ablation Device
  • Rollerball Ablation/Resection 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
Feb 29, 2012
Primary completion
Dec 31, 2014
Completion
Mar 1, 2018
Last update posted
Apr 17, 2018

2012 – 2018

United States locations

U.S. sites
8
U.S. states
7
U.S. cities
8
Facility City State ZIP Site status
New Horizons Women's Care Chandler Arizona 85224
Women's Health Research Phoenix Arizona 85015
Basinski, LLC Newburgh Indiana 47630
Cypress Medical Research Center, LLC Wichita Kansas 67226
Minnesota Gynecology and Surgery Edina Minnesota 55435
Mercy Clinic Minimally Invasive Gynecology St Louis Missouri 63141
Tennessee Women's Care PC Nashville Tennessee 37203
Baylor Research Institute 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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01569763, 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 17, 2018 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01569763 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →