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Clinical Trial Summary

The objective of this clinical investigation is to provide the first and preliminary clinical data to study the safety and efficacy of male circumcision where the dry circumcision method is employed.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT00572754
Study type Interventional
Source Progressus
Contact Kasonde Bowa, MD
Phone 260 97 84 93 0
Email kbowa@yahoo.com
Status Recruiting
Phase Phase 2
Start date November 2007
Completion date March 2008

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