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Completed Not applicable Interventional Accepts healthy volunteers

FemBloc® Permanent Contraception - Early Pivotal Trial

ClinicalTrials.gov ID: NCT03433911

Public ClinicalTrials.gov record NCT03433911. 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, 8:20 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

BLOC: Prospective Multi-Center Office Based Bi-Lateral Tubal Occlusion Trial for Female Permanent Contraception

Study identification

NCT ID
NCT03433911
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Femasys Inc.
Industry
Enrollment
240 participants

Conditions and interventions

Conditions

Interventions

  • FemBloc Device
  • Laparoscopic bilateral tubal sterilization Procedure

Device · Procedure

Eligibility (public fields only)

Age range
21 Years to 45 Years
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
Feb 1, 2018
Primary completion
Jan 30, 2020
Completion
Feb 9, 2025
Last update posted
Feb 26, 2026

2018 – 2025

United States locations

U.S. sites
12
U.S. states
11
U.S. cities
12
Facility City State ZIP Site status
New Horizons Clinical Trials Chandler Arizona 85224
Stanford University Stanford California 94305
Altus Research Inc. Lake Worth Florida 33461
Rosemark Womencare Specialists Idaho Falls Idaho 83404
Women's Health Advantage Fort Wayne Indiana 46825
Rutgers, The State University of New Jersey Newark New Jersey 07103
Columbia University Medical Center New York New York 10032
Wake Research Associates, LLC Raleigh North Carolina 27612
University Hospitals Cleveland Medical Center Beachwood Ohio 44122
Amy Brenner MD & Associates Mason Ohio 45069
Chattanooga Medical Research LLC Chattanooga Tennessee 37404
University of Utah Salt Lake City Utah 84132

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 NCT03433911, 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 26, 2026 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03433911 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →