Cohort Field Study to Assess the Safety and Efficacy of the PrePex Device for Non-Surgical Circumcision When Performed by Nurses

This study has been completed.
Sponsor:
Collaborator:
Rwanda Biomedical Center
Information provided by (Responsible Party):
Vincent Mutabazi, Ministry of Health, Rwanda
ClinicalTrials.gov Identifier:
NCT01434628
First received: September 10, 2011
Last updated: August 9, 2013
Last verified: August 2013
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study has been completed.
  Study Completion Date: December 2011
  Primary Completion Date: November 2011 (Final data collection date for primary outcome measure)