Pilot Bi-Lateral Tubal Occlusion Trial for Female Permanent Contraception

NACompletedINTERVENTIONAL
Enrollment

49

Participants

Timeline

Start Date

March 15, 2017

Primary Completion Date

February 27, 2018

Study Completion Date

March 14, 2023

Conditions
Contraception
Interventions
DEVICE

FemBloc® Permanent Contraceptive System

The FemBloc Permanent Contraceptive System consists of treatment with a Delivery System and Biopolymer, and a confirmation test with the FemChec® Tubal Occlusion Confirmation device as part of a sonographic hysterosalpingogram (Sono HSG).

Trial Locations (4)

10032

New York Presbyterian Hospital - Columbia University Medical Center, New York

27599

University of North Carolina, Chapel Hill, Chapel Hill

33461

Altus Research Inc., Lake Worth

37404

Chattanooga Medical Research, Chattanooga

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Femasys Inc.

INDUSTRY

NCT03067272 - Pilot Bi-Lateral Tubal Occlusion Trial for Female Permanent Contraception | Biotech Hunter | Biotech Hunter