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Completed Not applicable Interventional Accepts healthy volunteers

Study to Assess Outcomes in Women Undergoing Either Hysteroscopic Sterilization (Essure®) or Laparoscopic Tubal Sterilization

ClinicalTrials.gov ID: NCT03127722

Public ClinicalTrials.gov record NCT03127722. 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 May 13, 2026, 11:12 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

An Open-label, Non-randomized, Prospective Observational Cohort Study to Assess Post-procedural Outcomes in Two Cohorts of Women Who Chose to Undergo Either Hysteroscopic Sterilization (Essure®) or Laparoscopic Tubal Sterilization

Study identification

NCT ID
NCT03127722
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Bayer
Industry
Enrollment
990 participants

Conditions and interventions

Conditions

Interventions

  • Blood draw Procedure
  • ESSURE (BAY1454032) Device
  • Laparoscopic tubal sterilization Procedure

Procedure · Device

Eligibility (public fields only)

Age range
21 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
May 2, 2017
Primary completion
Dec 30, 2024
Completion
Dec 30, 2024
Last update posted
Jan 7, 2025

2017 – 2024

United States locations

U.S. sites
57
U.S. states
27
U.S. cities
50
Facility City State ZIP Site status
New Horizons Women's Care Chandler Arizona 85224
Precision Trials, AZ, LLC Phoenix Arizona 85032
Visions Clinical Research - Tucson Tucson Arizona 85712
Eclipse Clinical Research Tucson Arizona 85745-2696
Baptist Health Center for Clinical Research Little Rock Arkansas 72205-6325
United Clinical Research Huntington Beach California 90255
Orange Coast Women's Medical Group - Laguna Hills Office Laguna Hills California 92653
Physicians Research Options, LLC Lakewood Colorado 80228
The Women's Health Group, P.C. Thornton Colorado 80229-4388
M & O Clinical Research, LLC Fort Lauderdale Florida 33316
Altus Research Lake Worth Florida 33461
Universal Axon Clinical Research Miami Florida 33166
Physician Care Clinical Research Sarasota Florida 34239
Clinical Research Prime, LLLP Idaho Falls Idaho 83402-3344
John H Stroger Jr. Hospital of Cook County Chicago Illinois 60612
Women's Health Advantage Fort Wayne Indiana 46825
IU Health University Hospital Indianapolis Indiana 46202
Office of Dr. Cindy Basinski, LLC Newburgh Indiana 47630
Women's Health Care, PC Newburgh Indiana 47630
The Iowa Clinic, PC West Des Moines Iowa 50266-8289
University of Kentucky Albert B. Chandler Hospital Lexington Kentucky 40536-0001
Horizon Research Group of Opelousas, LLC Eunice Louisiana 70535
Mid-Atlantic Permanente Research Institute Rockville Maryland 20852
Tufts Medical Center Boston Massachusetts 02111
Women's Integrated Health Care, PC Grand Blanc Michigan 48439
Jersey Shore University Medical Center Neptune City New Jersey 07753
Columbia University Medical Center New York New York 10032
Unified Women's Clinical Research, LLC Greensboro North Carolina 27401-1207
Women's Health Alliance Raleigh North Carolina 27607
Unified Women's Clinical Research Winston-Salem North Carolina 27103-1749
Wake Forest Baptist Health Winston-Salem North Carolina 27157-1009
Seven Hills Women's Health Centers Cincinnati Ohio 45242
MetroHealth Medical Center Cleveland Ohio 44109-1998
Ohio State University Columbus Ohio 43210
Columbus OB-GYN/Radiant Research Columbus Ohio 43213
Complete Healthcare for Women, Inc. Columbus Ohio 43231
Wright State Physicians Health Center Dayton Ohio 45405-4534
HWC Women's Research Center Englewood Ohio 45322
HillTop Obstetrics & Gynecology Franklin Ohio 45005-2593
Amy Brenner, MD & Associates, LLC Mason Ohio 45040
AC Clinical Research Tiffin Ohio 44883-2820
Oklahoma University Oklahoma City Oklahoma 73104
Oregon Health and Science University Portland Oregon 97239
St. Luke's Hospital - Allentown Campus Allentown Pennsylvania 18104-9701
Women's Health Care Group of PA Pottstown Pennsylvania 19464
Reading Hospital West Reading Pennsylvania 19611
Women & Infants Hospital (OGCC) Providence Rhode Island 02905
Palmetto Clinical Research (PCR) Charleston South Carolina 29406-9126
OB-GYN Centre of Excellence Chattanooga Tennessee 37404
University of Tennessee Medical Center Knoxville Tennessee 37920
Ben Taub General Hospital Houston Texas 77030
The Woman's Hospital of Texas Houston Texas 77054
Southeast Texas Family Planning and Cancer Screening Houston Texas 77074
Brown Stone Clinical Trials, LLC Irving Texas 75061
Tanner Clinic Layton Utah 84041-8803
Women's Healthcare Associates, LLC - Tualatin Pleasant Grove Utah 84062-4097
Tidewater Clinical Research, Inc. Virginia Beach Virginia 23456

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 NCT03127722, 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 Jan 7, 2025 · Synced May 13, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03127722 live on ClinicalTrials.gov.

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