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Acceptability of Depo-subQ Provera 104 in Uniject Versus Intramuscular Depo-Provera Among HIV-positive Women and Family Planning Providers in Rakai, Uganda

NCT01578447 NA COMPLETED

The purpose of this study is to assess acceptability and side effects of a low-dose injectable contraceptive formulation which is delivered under the skin (subcutaneously), as compared with injectable contraception delivered into the muscle (intramuscularly) among adult HIV-positive women who attend mobile clinics for HIV care and wish to use injectable contraception. The investigators will also assess experiences experiences delivering these two types of injections among health care providers working within the HIV care clinics.

Details

Lead sponsorJohns Hopkins Bloomberg School of Public Health
PhaseNA
StatusCOMPLETED
Enrolment356
Start date2012-04
Completion2013-03

Conditions

Interventions

Primary outcomes

Countries

Uganda