NCT01434628View on ClinicalTrials.gov

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

NACompletedINTERVENTIONAL

Enrollment

590

Participants

Timeline

Start Date

July 31, 2011

Primary Completion Date

November 30, 2011

Study Completion Date

December 31, 2011

Conditions

Male CircumcisionHIV Prevention

Interventions

DEVICE

PrePex™ device

PrePex™ device for adult male circumcision. The PrePex™ device facilitates adult male circumcision that is bloodless with no anesthesia and no sutures

Trial Locations (1)

Unknown

Kanombe Military Hospital, Kigali

All Listed Sponsors

lead

Ministry of Health, Rwanda

OTHER_GOV

NCT01434628 - Cohort Field Study to Assess the Safety and Efficacy of the PrePex Device for Non-Surgical Circumcision When Performed by Nurses | Biotech Hunter | Biotech Hunter