A Pivotal Study to Assess the Safety and Efficacy of The PrePex System, a Male Circumcision Device and Methodology for Rapid Scale up of Painless and Bloodless National Circumcision Programs, in Urban and Remote Rural Settings

This study has been completed.
Sponsor:
Collaborator:
Ministry of Defence, Rwanda
Information provided by:
Ministry of Health, Rwanda
ClinicalTrials.gov Identifier:
NCT01150370
First received: June 23, 2010
Last updated: January 10, 2011
Last verified: December 2010
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study has been completed.
  Study Completion Date: December 2010
  Primary Completion Date: December 2010 (Final data collection date for primary outcome measure)