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

HIV Prevention Clinical Trial

Official title:
Safety and Acceptability Study of Non-Surgical Male Circumcision Device for Adult Male Population When Removing the Foreskin Shortly After Placement of Device Performed at Lusaka and Livingstone, Zambia

Clinical Trial 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.

Clinical Trial Description

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.

Five hundred (500) males scheduled for voluntary circumcision performed by clinicians or nurses using the PrePex.

Theses clinicians and nurses have already been trained in the Prepex procedure and will undergo further training in the modification to the technique. Study duration per participant will be up to 8 weeks and will include three follow up visits and one phone call follow up. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03132285
Study type Interventional
Source Ministry of Health, Zambia
Contact
Status Completed
Phase N/A
Start date March 11, 2017
Completion date June 17, 2017
View Details
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