Study to Assess Outcomes in Women Undergoing Either Hysteroscopic Sterilization (Essure®) or Laparoscopic Tubal Sterilization
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.
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
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
This study is designed to assess post-procedural outcomes for women who chose to undergo either hysteroscopic sterilization (Essure®) or laparoscopic tubal sterilization, including: * Pelvic and/or lower abdominal pain * Abnormal uterine bleeding * Surgical intervention (including "insert removal" and hysterectomy) * Allergic, hypersensitivity, or autoimmune-like reactions
Study identification
- NCT ID
- NCT03127722
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Not applicable
- 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 3, 2017 (Actual)
- Primary completion
- Dec 31, 2024 (Actual)
- Completion
- Dec 31, 2024 (Actual)
- Last update posted
- May 22, 2026
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 May 22, 2026 · 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 NCT03127722 live on ClinicalTrials.gov.