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Completed No phase listed Observational Results available

A Study to Evaluate the Effectiveness of Essure Post-NovaSure Radiofrequency Endometrial Ablation Procedure Following a Successful Essure Confirmation Test

ClinicalTrials.gov ID: NCT01740687

Public ClinicalTrials.gov record NCT01740687. 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 22, 2026, 3:36 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

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

The purpose of the post approval study is to evaluate the effectiveness and safety of the Essure System when a NovaSure Endometrial Ablation procedure is performed following a successful Essure Confirmation Test.

Study identification

NCT ID
NCT01740687
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Bayer
Industry
Enrollment
211 participants

Conditions and interventions

Interventions

Device · Procedure

Eligibility (public fields only)

Age range
21 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
Nov 13, 2012 (Actual)
Primary completion
May 17, 2021 (Actual)
Completion
Jun 14, 2021 (Actual)
Last update posted
Feb 6, 2023

2012 – 2021

United States locations

U.S. sites
17
U.S. states
15
U.S. cities
17
Facility City State ZIP Site status
Not listed Aurora Colorado 80045 —
Not listed Ocala Florida 34471 —
Not listed Decatur Illinois 62526 —
Not listed Fort Wayne Indiana 46825 —
Not listed Newburgh Indiana 47630 —
Not listed Easton Maryland 21601 —
Not listed Grand Blanc Michigan 48439 —
Not listed Maplewood Minnesota 55109 —
Not listed Las Vegas Nevada 89102 —
Not listed Neptune City New Jersey 07753 —
Not listed Winston-Salem North Carolina 27103 —
Not listed Englewood Ohio 45322 —
Not listed Mason Ohio 45040 —
Not listed Pottstown Pennsylvania 19464 —
Not listed Nashville Tennessee 37232 —
Not listed Norfolk Virginia 23507 —
Not listed Spokane Washington 99204 —

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 NCT01740687, 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 6, 2023 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01740687 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →