Skip to content

Effect of Male Circumcision on HIV Incidence (ANRS 1265)

Effect of Safe Male Circumcision on Incidence of Infection by HIV, HSV-2 and of Genital Ulceration

Status
Terminated
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00122525
Enrollment
3274
Registered
2005-07-22
Start date
2002-07-31
Completion date
2005-07-31
Last updated
2009-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Herpes Genitalis, HIV Infections, Venereal Diseases

Keywords

HIV, Male circumcision, Prevention, HSV-2, Africa, Sexual behavior

Brief summary

Observational studies suggest that male circumcision may provide protection against HIV-1 infection. A randomized, controlled, intervention trial was conducted in a general population of South Africa to test this hypothesis.

Detailed description

This study is a randomized controlled intervention trial. This multi-centre study will take place in 3 centers located around Johannesburg, in the areas of Orange Farm, Sebokeng and Evaton. The intervention group patients (circumcised at the beginning of the trial) and the control group (uncircumcised men) will be followed during 21 months (from M.0 to M. 21). Randomization and medicalized circumcision will be performed at M.0 in the intervention group and might be optional in the control group at end of study. The medicalized circumcision effectiveness will be evaluated on and after M.3 (3 months after medicalized circumcision). Incidences (of HIV, HSV-2 infections and genital ulcer disease) will be compared from M.3 to M.21 between the intervention group and the control group. An intermediate analysis will take place at M. 12.

Interventions

PROCEDUREMale Circumcision

Sponsors

French National Agency for Research on AIDS and Viral Hepatitis
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 24 Years
Healthy volunteers
Yes

Inclusion criteria

* Uncircumcised men aged 18-24 years * Be in good general condition with normal physical and genital examinations * Consenting to participate in the trial and to sign an informed consent * Consenting to randomization of the medicalized circumcision schedule (performed at the beginning of study for the treated group, optional at the end of study for the control group) * Consenting to avoid sexual contact (except with condom protection) during the 6 weeks following the medicalized circumcision * Consenting to blood tests at M.0, M.3, M.12 and M.21 tested for HIV, HSV-2 and syphilis.

Exclusion criteria

* Men with AIDS * Men with contraindication for circumcision * Men thinking of moving away from the trial sites within the 21 months following inclusion * Men with clinical sexually transmitted diseases (STDs) (those men could be included after treatment)

Design outcomes

Primary

MeasureTime frame
Measure the protective effect of medicalized male circumcision on HIV infectionM3, M12 and M21

Secondary

MeasureTime frame
Measure the protective effect on infections by the genital herpes agent Herpes simplex virus type 2 (HSV-2)M3, M12 and M21
Measure the protective effect on the incidence of genital ulcer diseaseM3, M12 and M21

Countries

South Africa

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 3, 2026