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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 Jul 22, 2026, 3:22 PM EDT

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

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

  • ESS305 (Essure, BAY1454032) Device
  • NovaSure Procedure

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 12, 2012
Primary completion
May 16, 2021
Completion
Jun 13, 2021
Last update posted
Feb 5, 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 5, 2023 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01740687 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →