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Hormonal Birth Control and the Risk of Acquiring HIV

This study has been completed.

Sponsors and Collaborators: National Institute of Child Health and Human Development (NICHD)
National Institute of Allergy and Infectious Diseases (NIAID)
Information provided by: National Institute of Allergy and Infectious Diseases (NIAID)
ClinicalTrials.gov Identifier: NCT00006324
  Purpose

The purpose of this study is to find out whether hormonal birth control increases, decreases, or does not change the risk of women becoming infected with HIV.

Sexual intercourse between men and women is the main way HIV is transmitted. About 90 percent of HIV infections in women are caused by sexual intercourse. Also, hormonal birth controls are widely used. This study hopes to find out whether hormonal birth control changes the risk of women becoming infected with HIV.


Condition Intervention
HIV Infections
Drug: Ethinyl estradiol/levonorgestrel
Drug: Medroxyprogesterone acetate

MedlinePlus related topics:   AIDS    Birth Control   

ChemIDplus related topics:   Depogen    Estradiol    Estradiol 3-benzoate    Estradiol acetate    Estradiol cypionate    Estradiol dipropionate    Estradiol valerate    Polyestradiol phosphate    Ethinyl estradiol    Medroxyprogesterone    Medroxyprogesterone 17-acetate    Levonorgestrel   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment
Official Title:   Hormonal Contraception and the Risk of HIV Acquisition

Further study details as provided by National Institute of Allergy and Infectious Diseases (NIAID):

Estimated Enrollment:   6360
Study Start Date:   December 1999
Estimated Study Completion Date:   December 2002

Detailed Description:

Heterosexual intercourse is the primary mode of HIV transmission worldwide and accounts for about 90% of HIV infections in women. Hormonal contraceptives including COCs and injectables are among the most widely used contraceptives in the world. Understanding the impact of hormonal contraception on HIV transmission is a critical unanswered public health question. Because of the critical nature of this issue to women of reproductive age worldwide, a methodologically sound study must be undertaken. It must be determined if hormonal contraceptive use increases the risk of HIV infection and the magnitude of the association, if it exists.

This study takes place in Thailand, Uganda, and Zimbabwe. HIV-seronegative women continue using their current birth control method (low dose COC, DMPA injections, or non-hormonal contraceptive methods [condoms, sterilization, or no modern contraception method]) for the duration of the study. They are followed every 12 weeks for a minimum of 15 months and a maximum of 24 months, or until seroconversion. Pelvic exams, including Pap smears, are done, blood samples are drawn, and vaginal and cervical specimens are tested for any sexually transmitted diseases (STDs). Women are provided with free treatment for any STDs that are diagnosed. They complete a questionnaire on sexual behavior and contraceptive history; counseling on contraceptive use and reducing HIV risk is provided.

  Eligibility
Ages Eligible for Study:   16 Years to 35 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria

Women may be eligible for this study if they:

  • Are 16 to 35 years of age.
  • Attend family planning and maternal and child health clinics in Zimbabwe, Thailand, or Uganda.
  • Have been using low-dose birth control pills, DMPA injections, or non-hormonal birth control (condoms, sterilization, or no modern birth control method) for at least 3 months and plan to continue using the same type of birth control for a year.
  • Are HIV-negative.
  • Are sexually active.
  • Are at least 4.5 months after delivery, if they have given birth.
  • Agree to all study procedures, including HIV testing every 3 months, follow-up clinic visits, and home visits if they fail to return for follow-up.
  • Have a home address where they can be reached for follow-up visits.

Exclusion Criteria

Women will not be eligible for this study if they:

  • Are pregnant or plan to try to become pregnant in the next year. Women who become pregnant after enrolling in the trial will not be discontinued.
  • Are not currently using low-dose birth control pills or DMPA for birth control but have used low-dose birth control pills within the last 3 months, or DMPA for birth control within the previous 6 months.
  • Are HIV-indeterminate or HIV-positive.
  • Have used an IUD for birth control in the last month.
  • Have used non-study types of birth control (such as Norplant, NET-EN, or progestin-only pills) within the last 3 months.
  • Have had a full hysterectomy.
  • Have had an abortion or miscarriage within the last month.
  • Have had a blood transfusion within the last 3 months.
  • Were previously or are currently in an HIV vaccine trial.
  • Injected illegal drugs within the last 3 months.
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00006324

Locations
United States, North Carolina
Amy Lovvorn    
      Research Triangle Park, North Carolina, United States, 27709

Sponsors and Collaborators

Investigators
Study Chair:     Charles Morrison    
Study Chair:     Barbra Richardson    
Principal Investigator:     Sungwal Rugpao    
Principal Investigator:     Roy Mugerwa    
Principal Investigator:     Francis Mmiro    
Principal Investigator:     Tsungai Chipato    
  More Information


Haga clic aquí para ver información sobre este ensayo clínico en español.  This link exits the ClinicalTrials.gov site
 

Study ID Numbers:   HIVNET 021
First Received:   October 2, 2000
Last Updated:   August 6, 2008
ClinicalTrials.gov Identifier:   NCT00006324
Health Authority:   United States: Federal Government

Keywords provided by National Institute of Allergy and Infectious Diseases (NIAID):
HIV Seronegativity  
Delayed-Action Preparations  
Risk Factors  
Prevalence  
Contraceptive Agents, Female
Contraceptives, Oral, Combined
Medroxyprogesterone 17-Acetate

Study placed in the following topic categories:
Sexually Transmitted Diseases, Viral
Medroxyprogesterone 17-Acetate
Acquired Immunodeficiency Syndrome
Estradiol valerate
Ethinyl Estradiol
Estradiol 17 beta-cypionate
Estradiol
Immunologic Deficiency Syndromes
Virus Diseases
HIV Infections
Estradiol 3-benzoate
Levonorgestrel
Sexually Transmitted Diseases
Medroxyprogesterone
Polyestradiol phosphate
Retroviridae Infections

Additional relevant MeSH terms:
RNA Virus Infections
Estrogens
Slow Virus Diseases
Antineoplastic Agents, Hormonal
Immune System Diseases
Antineoplastic Agents
Contraceptive Agents
Contraceptives, Oral
Physiological Effects of Drugs
Hormones, Hormone Substitutes, and Hormone Antagonists
Contraceptive Agents, Female
Reproductive Control Agents
Contraceptive Agents, Male
Infection
Hormones
Pharmacologic Actions
Therapeutic Uses
Lentivirus Infections
Contraceptives, Oral, Synthetic

ClinicalTrials.gov processed this record on October 03, 2008




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