A Randomized Trial of IUD Versus Hormonal Contraception in HIV-infected Women in Zambia
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|ClinicalTrials.gov Identifier: NCT00336245|
Recruitment Status : Completed
First Posted : June 13, 2006
Last Update Posted : March 6, 2015
|Condition or disease||Intervention/treatment||Phase|
|Pregnancy HIV Infection||Device: Copper T Intrauterine Contraceptive Device Drug: Hormonal Contraception||Phase 3|
In the year 2000, there were over 37, 000 new acceptors of family planning in the Lusaka District Clinics. A variety of methods were prescribed, including combined oral contraceptive pills, injectable progestins, the intrauterine copper device, condoms, and others. The most recent sentinel survey of reproductive age women estimated that approximately 30% of reproductive age women in Lusaka are HIV-infected. Since voluntary HIV counseling and testing is not yet universally available in many of the district clinics, women receive all different types of contraception regardless of their HIV status.
There is some observational data published recently that suggests hormonal contraception may increase HIV viral load in the female genital tract and potentially increase HIV transmission to the male partner. By contrast, barrier methods have historically been very unpopular in stable couples and are not used consistently in many cases despite intensive counseling. The IUCD represents one of the most inexpensive and effective methods of birth control available in Lusaka. However, it has not been studied adequately to make policy recommendations regarding its use in HIV infected women. The purpose of this study will be to evaluate safety and acceptability of the IUCD versus hormonal methods of contraception in HIV-infected and uninfected women in Lusaka. Specifically, we will 1) compare the contraceptive effectiveness of the IUCD to the standard practices of user-chosen hormonal contraception, 2) compare the rates of pelvic infection between IUD and hormonal contraceptive users, and 3) compare rates of method discontinuation.
Patients who have a continuing second trimester pregnancy, serologically confirmed HIV infection, a desire for 24 months of contraception, and a willingness to be randomly assigned either an IUCD or hormonal contraception postpartum will be screened at 32 weeks in their pregnancies to receive either an IUCD or user chosen hormonal contraception postpartum. Women will then be seen at postpartum weeks 4-6 for method randomization and then at months 6, 12, 18 and 24 to monitor pregnancy, continuation of method, side effects and any other problems. Women will be encouraged to return for problems at any time. At least once yearly, women will have a complete physical exam. CD4 and HIV clinical status will be monitored regularly.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||600 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Randomized Trial of IUD Versus Hormonal Contraception in HIV-infected Women in Zambia|
|Study Start Date :||June 2002|
|Primary Completion Date :||October 2005|
|Study Completion Date :||October 2005|
|Experimental: Copper T Intrauterine Contraceptive Device||Device: Copper T Intrauterine Contraceptive Device|
|Active Comparator: Hormonal Contraception||Drug: Hormonal Contraception|
- Incident pregnancy
- Method discontinuation rates
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00336245
|Principal Investigator:||Jeffrey Stringer, MD||University of Alabama at Birmingham|