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FemBloc® Permanent Contraception - Early Pivotal Trial — BLOC  

Contraception Clinical Trial

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

Clinical Trial Summary

Prospective, multi-center, international, non-randomized, two-arm study of subjects undergoing either FemBloc or laparoscopic bilateral tubal sterilization (Control). The FemBloc group total study duration will be approximately 65 months. The laparoscopic tubal sterilization (Control) group total study duration will be approximately 62 months.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03433911
Study type Interventional
Source Femasys Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date February 2, 2018
Completion date January 2025
View Details
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