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Male Circumcision and HIV Rates in Kenya - Article


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Male Genital Disorders

Penile Disorders; Testicular Disorders 




Clinical Trial: Male Circumcision and HIV Rates in Kenya

This study is currently recruiting patients.

Sponsored by: National Institute of Allergy and Infectious Diseases (NIAID)
Information provided by: National Institute of Allergy and Infectious Diseases (NIAID)

Purpose

The Luo tribe of Kisumu, Kenya, does not traditionally practice male circumcision (MC). This study will work with the Luo tribe to test the effectiveness of MC on reducing the risk of HIV infections in young men.

Condition Treatment or Intervention Phase
HIV Infections
 Procedure: male circumcision
Phase III

MedlinePlus related topics:  AIDS

Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Placebo Control, Factorial Assignment, Safety/Efficacy Study

Official Title: Trial of Male Circumcision to Reduce HIV Incidence

Further Study Details: 

Expected Total Enrollment:  3000

Study start: February 2002;  Expected completion: February 2007

Since 1989, numerous epidemiological studies have reported a significant association between lack of male circumcision (MC) and risk for HIV infection through heterosexual intercourse. These results have led to calls for male circumcision to be considered as an additional HIV prevention strategy. However, there is a consensus among the international health community that a randomized controlled trial of MC is needed to control for possible confounding factors. Additionally, known risks associated with MC need further investigation. This study will assess the effectiveness of male circumcision in reducing HIV incidence and will evaluate complications of the MC procedure, changes in sexual behavior following circumcision, and the biological mechanisms by which the foreskin may increase HIV susceptibility. The study will be conducted in Kisumu, Kenya, where the Luo tribe is the main ethnic group and less than 10% of adult men are circumcised.

Uncircumcised men aged 18 to 24 years old will be offered voluntary HIV counseling and testing. HIV negative men will be asked to enroll in the study. All study participants will be interviewed to obtain socio-demographic information and assess behavioral risk factors. Participants will be examined for significant medical conditions. All men will be counseled in strategies to reduce their risk for HIV infection. Consenting men will be randomly assigned to either the treatment (circumcised) arm or the control (uncircumcised) arm of the study. After circumcision, men will be monitored for complications. They will be counseled to abstain from sex until healing is complete. Follow-up visits will occur every 6 months for 2 years. Uncircumcised men will be offered circumcision at the end of follow-up.

The primary study endpoints will be HIV incidence and surgical complications. Additional outcomes will be the incidence of other sexually transmitted diseases and behavioral risks. Additional laboratory studies of foreskin tissue will evaluate the number and density of specialized cells rich in HIV receptors in order to illuminate the biological mechanisms by which presence of foreskin may increase HIV susceptibility.

Eligibility

Ages Eligible for Study:  18 Years   -   24 Years,  Genders Eligible for Study:  Male

Accepts Healthy Volunteers

Criteria

Inclusion Criteria

  • HIV uninfected and willing to be tested
  • Live in Kisumu District, Kenya
  • Uncircumcised but willing to be circumcised
  • At least one sexual partner in the 12 months prior to study entry

Location and Contact Information


Kenya
      UNIM Clinic, Kisumu,  Kenya; Recruiting
Kwango Agot, PhD  0733-912603 
Kwango Agot, PhD,  Sub-Investigator

Study chairs or principal investigators

Robert C. Bailey, PhD, MPH,  Principal Investigator,  University of Illinois   

More Information

Study ID Numbers:  5U01AI050440-02
Record last reviewed:  November 2004
Last Updated:  November 2, 2004
Record first received:  April 23, 2003
ClinicalTrials.gov Identifier:  NCT00059371
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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December 5, 2009



Page Updated: October 3, 2005
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