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Safety and Acceptability Study of PrePex Device When Removing the Foreskin Shortly After Placement of Device

NCT03132285 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 500

Last updated 2017-09-07

No results posted yet for this study

Summary

To assess the safety and acceptability of the non-surgical PrePex device among healthy adult male participants scheduled for voluntary medical male circumcision when removing the foreskin shortly after device placement.

Conditions

  • HIV Prevention

Interventions

DEVICE

PrePex

Prepex is a non surgical male circumcision device

Sponsors & Collaborators

  • Ministry of Health, Zambia

    lead OTHER_GOV

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
13 Years
Max Age
49 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-03-11
Primary Completion
2017-04-22
Completion
2017-06-17

Countries

  • Zambia

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 NCT03132285 on ClinicalTrials.gov