Rapid HIV Tests for Women Late in Pregnancy and During Labor
|ClinicalTrials.gov Identifier: NCT00046436|
Recruitment Status : Terminated
First Posted : October 1, 2002
Last Update Posted : June 3, 2013
|Condition or disease|
A simple HIV test design and easily interpretable, fast results are logistical advantages in clinical settings such as the labor and delivery unit. A fast test result means that a woman can make important choices about her and her baby's medical care before she delivers her baby. If a woman finds out she has HIV, she can decide to take antiretroviral drugs before delivery to decrease the risk of passing HIV to her baby. These advantages are also important for women with little or no prenatal care who present for care late in pregnancy, but may not be inclined to return for a standard test result or adhere to subsequent prenatal visits.
Eligible women who elect to participate in this study will be enrolled in either the Late Presenter Group (women who are not in active labor, and for whom delivery is not imminent) or the Peripartum Group (women who are in active labor with anticipation of delivery within 24 hours). Step I for all women will include rapid HIV testing with OraQuick HIV 1/2 and standard testing with enzyme-linked immunosorbant assay (EIA) or Western blot. Women with a positive HIV test and their infants will be offered preventative antiretroviral therapy and enrollment into Step II. Step II will include clinical evaluations, laboratory evaluations, and an adherence assessment for the women and their infants. Women in the Late Presenter Group who participate in Step II will have one prenatal visit, a visit at labor and delivery, and three postpartum visits. Women in the Peripartum Group who participate in Step II will have three postpartum visits. All infants in Step II will have five study visits through 24 weeks of age.
All antiretroviral drugs will be obtained by prescription and will not be provided through this study.
|Study Type :||Observational|
|Estimated Enrollment :||7500 participants|
|Official Title:||Mother-Infant Rapid Intervention at Delivery (MIRIAD)|
|Study Completion Date :||March 2004|
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00046436
|United States, Pennsylvania|
|Univ. of Pennsylvania Health System, Hosp. of the Univ. of Pennsylvania|
|Philadelphia, Pennsylvania, United States, 19104|
|Study Chair:||Robert Maupin, Jr., MD||Louisiana State University Health Sciences Center in New Orleans|