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Phase II Trial to Evaluate the Safety and Efficacy of the Dry Circumcision Method

NCT00572754 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 15

Last updated 2007-12-13

No results posted yet for this study

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.

Conditions

  • Circumcision
  • Male

Interventions

PROCEDURE

Circumcision

Circumcision by tying a ligature around the foreskin.

Sponsors & Collaborators

  • Progressus

    lead OTHER

Principal Investigators

  • Bertran Auvert, MD, PhD · UVSQ-INSERM-France

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-11-30
Completion
2008-03-31

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 NCT00572754 on ClinicalTrials.gov