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Safety and Efficacy of the PrePex Device Circumcision When Performed by Nurses

NCT01956383 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 603

Last updated 2013-10-08

No results posted yet for this study

Summary

The protocol, approved by the Medical Research Council, was issued to assess the safety and efficacy of the non-surgical device for applying it to the national scale up of adult male circumcision in Zimbabwe

Conditions

  • Circumcision Adult
  • HIV CDC Category B2

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

Sponsors & Collaborators

  • Ministry of Health and Child Welfare, Zimbabwe

    lead OTHER

Principal Investigators

  • Gerald Gwinji, MBChB, MPH · PS- MoHCW

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
30 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-04-30
Primary Completion
2012-09-30
Completion
2012-09-30

Countries

  • Zimbabwe

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01956383 on ClinicalTrials.gov