The protocol, approved by the Rwanda National Ethical Committee, was issued to assess the safety and efficacy of the circumcision device for applying it to the national scale up of adult male circumcision in Rwanda
Multiple randomized and controlled studies (WHO, USAID, UNAIDS) have proven that circumcised men in high risk areas reduce their risk of HIV infection by 60%. The Government of Rwanda has ranked HIV prevention as a top priority item, and wishes to decrease the HIV incidence in the country by 50%. As part of a holistic HIV prevention approach, we decided to embark upon a process of national scale up of adult male circumcision. The national HIV prevention plan calls for voluntary MC of 2 million adults by the end of 2012. The PrePex System was designed to enable safe, effective, painless and bloodless male circumcision programs, to support global public health efforts to stop the spread of HIV. The PrePex System includes a simple, disposable device that is easy to use and can be deployed by minimally trained healthcare professionals, in urban or rural settings, without the need for sterile, hospital settings. As such, The PrePex System places minimal burden on the existing health care infrastructure to accomplish national circumcision programs. The protocol, approved by the Rwanda National Ethical Committee, was issued to assess the safety and efficacy of the circumcision device for applying it to the national scale up of adult male circumcision in Rwanda.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
50
The PrePex System was designed to enable safe, effective, painless and bloodless male circumcision programs. The PrePex System includes a simple, disposable device that is easy to use and can be deployed by minimally trained healthcare professionals, without the need for sterile, hospital settings.
Kanombe Military Hospital
Kigali, Kigali, Rwanda
The efficacy and safety of The PrePex System for adult male circumcision in Rwanda
Outcome measures will include: Number of Participants with Adverse Events as a Measure of Safety, Pain as measured by Visual Analogue Scale (VAS), Wound healing rate.
Time frame: 4 week post-procedure follow up appointment and examination
Operational scalability to mass scale up program
Outome measure include: Duration required by diffrent personnel to perform the procedure Procedure performance by nurses
Time frame: four week post-procedure follow up appointment and examination
satisfaction & acceptability of patients
Outcome measure include: Quality of life and satisfaction questionnaire
Time frame: 4 weeks follow up
Guidelines for utility in scale up mass circumcision program
Outcome measure includes: Physicians questionnaire on the clinical and practical performance of the procedure
Time frame: 4 weeks follow up
compliance with post procedure instructions
Outcome measure include: Weekly follow up visits post procedure, compliance with post procedure instructions questionnaire
Time frame: 4 weeks follow up
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.