Rapid HIV Tests for Women Late in Pregnancy and During Labor
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Purpose
This study will look at how well the OraQuick HIV 1/2 Antibody rapid test works and how women accept being tested for HIV late in pregnancy and during labor. For women with positive test results, the study will look at whether or not these women accept anti-HIV drugs and which drugs they receive.
| Condition |
|---|
|
HIV Infections |
| Study Type: | Observational |
| Study Design: | Time Perspective: Prospective |
| Official Title: | Mother-Infant Rapid Intervention at Delivery (MIRIAD) |
| Estimated Enrollment: | 7500 |
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.
Eligibility| Ages Eligible for Study: | 13 Years and older |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
INCLUSION CRITERIA
Late Presenter Group:
- Unknown HIV serostatus
- >= 34 weeks gestation
Peripartum Group:
- Unknown HIV serostatus
- >= 24 weeks gestation
- In active labor or delivery expected within 24 hours
Infants:
- Maternal Step I enrollment
- Positive maternal OraQuick and/or EIA/Western blot result
EXCLUSION CRITERIA
Late Presenter Group:
- Previous or current antiretroviral therapy for treatment of HIV infection
- In active labor
- Evidence of ruptured membranes
Peripartum Group:
- Previous or current antiretroviral therapy for treatment of HIV infection
Contacts and Locations| United States, California | |
| Harbor-UCLA Med Ctr | |
| Torrance, California, United States, 90509 | |
| United States, District of Columbia | |
| Howard University Hospital | |
| Washington, District of Columbia, United States | |
| United States, Massachusetts | |
| Univ of Massachusetts Med School | |
| Worcester, Massachusetts, United States, 01655-0001 | |
| United States, New York | |
| New York Univ School of Medicine | |
| New York, New York, United States, 10016 | |
| United States, Pennsylvania | |
| St. Christophers Hosp for Children, Philadelphia | |
| Philadelphia, Pennsylvania, United States, 19134 | |
| Hahnemann University Hospital | |
| Philadelphia, Pennsylvania, United States, 19102-1192 | |
| Puerto Rico | |
| San Juan City Hosp | |
| San Juan, Puerto Rico, 00936-7344 | |
| University of Puerto Rico. Univ Childrens Hospital | |
| San Juan, Puerto Rico, 00936-5067 | |
| Study Chair: | Robert Maupin, Jr., MD | Louisiana State University Health Sciences Center in New Orleans |
More Information
Additional Information:
Publications:
| ClinicalTrials.gov Identifier: | NCT00046436 History of Changes |
| Other Study ID Numbers: | PACTG P1031 |
| Study First Received: | September 30, 2002 |
| Last Updated: | October 23, 2012 |
| Health Authority: | United States: Federal Government |
Keywords provided by National Institute of Allergy and Infectious Diseases (NIAID):
|
AIDS Serodiagnosis Pregnancy Complications, Infectious Anti-HIV Agents Disease Transmission, Vertical |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases |
Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases Slow Virus Diseases |
ClinicalTrials.gov processed this record on May 16, 2013