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Voluntary HIV Counseling, Testing, and Medication for Pregnant Women to Prevent Mother-to-Child HIV Transmission

Primary Purpose

HIV Infections

Status
Completed
Phase
Not Applicable
Locations
South Africa
Study Type
Interventional
Intervention
Intrapartum HIV counseling/testing
Postpartum HIV counseling/testing
Sponsored by
National Institute of Allergy and Infectious Diseases (NIAID)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV Infections focused on measuring HIV Seronegativity, Treatment Naive, Pediatric HIV, Perinatal Transmission

Eligibility Criteria

14 Years - undefined (Child, Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria for Women: Unknown HIV infection status At least seven months pregnant Women in active labor who have planned induction or Caesarean delivery or any other condition requiring planned delivery Inclusion Criteria for Infants: Mother is participating in study Mother is HIV infected Exclusion Criteria for Women: Women in labor who need immediate delivery Obstetrical emergencies in which the woman is medically unstable or requires emergency delivery Diagnosed fetal death or fetal condition requiring abortion

Sites / Locations

  • Hottentots Holland Hospital
  • Maccassar Community Health Clinic

Outcomes

Primary Outcome Measures

Time required to obtain informed consent
time from initiation of HIV pre-test counseling until test results are available
proportion of test evaluations completed before delivery
proportion of test evaluations completed before hospital discharge
proportion of women who agree to HIV testing
proportion of women identified as HIV infected during labor who accept ARV prophylaxis
proportion of women identified as HIV infected after birth who accept ARV therapy for their infants
timing of infant ARV prophylaxis initiation after birth, as a proportion of infants born to women identified as HIV infected after birth and as a continuous variable
timing of mother ARV initiation as a proportion of women identified as HIV infected during labor and as a continuous variable
qualitative measures (defined as available space, study staff allocation, support for counseling and testing, and women's perceptions and opinions of counseling and testing)

Secondary Outcome Measures

Proportion of women with undocumented HIV infection who are tested and determined to be HIV infected peripartum
performance of rapid HIV tests as measured by sensitivity and specificity
proportion of infants who complete the Week 6 study visit and efforts needed to accomplish this visit
proportion of infants being fed according to the method chosen at discharge (defined as exclusive breastfeeding, exclusive formula feeding, or mixed feeding), as reported by the mother at Week 6
proportion of HIV-exposed infants who acquire HIV infection during delivery and after birth
acceptance of HIV counseling and testing among clinical personnel at primary, secondary, and tertiary care facilities

Full Information

First Posted
June 4, 2004
Last Updated
October 26, 2012
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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1. Study Identification

Unique Protocol Identification Number
NCT00084045
Brief Title
Voluntary HIV Counseling, Testing, and Medication for Pregnant Women to Prevent Mother-to-Child HIV Transmission
Official Title
Mother Infant Rapid Intervention at Delivery (MIRIAD)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2012
Overall Recruitment Status
Completed
Study Start Date
November 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 2006 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

5. Study Description

Brief Summary
Voluntary HIV counseling and testing (VCT) and anti-HIV drugs for pregnant women and their newborns decrease rates of mother-to-child transmission (MTCT) of HIV. This study will determine the acceptability of HIV counseling and rapid testing prior to delivery and will compare the usefulness of VCT prior to birth versus after birth in preventing MTCT of HIV in pregnant women in Cape Town, South Africa. This study will also determine the acceptability and effectiveness of giving anti-HIV medications to prevent MTCT of HIV.
Detailed Description
Pediatric HIV infection is a major public health problem in South Africa, and is primarily caused by MTCT of HIV. Strategies to prevent MTCT have been successfully employed when a mother's HIV status is known. However, there is concern in South Africa that it is unethical to offer HIV testing to women in the intrapartum period when they are experiencing the physical and emotional stress of labor. This study will compare the acceptability and accuracy of intrapartum and postpartum VCT in pregnant women of unknown HIV status in Cape Town, South Africa. Pregnant women of unknown HIV status coming to a participating hospital to deliver will be asked to enter the trial. Women will be assigned to either intrapartum or postpartum VCT depending on the week during which they come to the hospital. The intervention (intrapartum or postpartum VCT) for the week will be randomly assigned and all women enrolling in the trial in a given week will receive the same intervention. All women will receive HIV counseling prior to testing. Women in the intrapartum VCT group who are HIV infected will receive antiretrovirals (ARV) prior to delivery to prevent MTCT, and their infants will receive ARV within 3 days of birth. Infants born to HIV infected women in the postpartum VCT group will receive ARV as soon as possible after confirmation of the mother's positive test. All women will receive post-test counseling prior to discharge. HIV VCT, medical history assessment, and physical exam will occur at study entry. A small subset of both HIV infected and uninfected mothers will be asked for their opinions regarding peripartum HIV VCT and MTCT prevention strategies during qualitative assessments. Infants will undergo physical exam within 2 days of birth, medical history assessment within 2 days of birth and at 3 additional times between 6 and 14 weeks of age, and HIV testing within 2 days of birth and at 2 additional times between 6 and 12 weeks of age.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
HIV Seronegativity, Treatment Naive, Pediatric HIV, Perinatal Transmission

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
283 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
Intrapartum HIV counseling/testing
Intervention Type
Procedure
Intervention Name(s)
Postpartum HIV counseling/testing
Primary Outcome Measure Information:
Title
Time required to obtain informed consent
Title
time from initiation of HIV pre-test counseling until test results are available
Title
proportion of test evaluations completed before delivery
Title
proportion of test evaluations completed before hospital discharge
Title
proportion of women who agree to HIV testing
Title
proportion of women identified as HIV infected during labor who accept ARV prophylaxis
Title
proportion of women identified as HIV infected after birth who accept ARV therapy for their infants
Title
timing of infant ARV prophylaxis initiation after birth, as a proportion of infants born to women identified as HIV infected after birth and as a continuous variable
Title
timing of mother ARV initiation as a proportion of women identified as HIV infected during labor and as a continuous variable
Title
qualitative measures (defined as available space, study staff allocation, support for counseling and testing, and women's perceptions and opinions of counseling and testing)
Secondary Outcome Measure Information:
Title
Proportion of women with undocumented HIV infection who are tested and determined to be HIV infected peripartum
Title
performance of rapid HIV tests as measured by sensitivity and specificity
Title
proportion of infants who complete the Week 6 study visit and efforts needed to accomplish this visit
Title
proportion of infants being fed according to the method chosen at discharge (defined as exclusive breastfeeding, exclusive formula feeding, or mixed feeding), as reported by the mother at Week 6
Title
proportion of HIV-exposed infants who acquire HIV infection during delivery and after birth
Title
acceptance of HIV counseling and testing among clinical personnel at primary, secondary, and tertiary care facilities

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria for Women: Unknown HIV infection status At least seven months pregnant Women in active labor who have planned induction or Caesarean delivery or any other condition requiring planned delivery Inclusion Criteria for Infants: Mother is participating in study Mother is HIV infected Exclusion Criteria for Women: Women in labor who need immediate delivery Obstetrical emergencies in which the woman is medically unstable or requires emergency delivery Diagnosed fetal death or fetal condition requiring abortion
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert Maupin, Jr., MD
Organizational Affiliation
Louisiana State University Health Science Center
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Mitchell Besser, MD
Organizational Affiliation
Department of Obstetrics and Gynecology, Groote Schuur Hospital Observatory
Official's Role
Study Chair
Facility Information:
Facility Name
Hottentots Holland Hospital
City
Cape Town
ZIP/Postal Code
7505
Country
South Africa
Facility Name
Maccassar Community Health Clinic
City
Cape Town
ZIP/Postal Code
7505
Country
South Africa

12. IPD Sharing Statement

Citations:
PubMed Identifier
16227795
Citation
Leroy V, Sakarovitch C, Cortina-Borja M, McIntyre J, Coovadia H, Dabis F, Newell ML, Saba J, Gray G, Ndugwa Ch, Kilewo Ch, Massawe A, Kituuka P, Okong P, Grulich A, von Briesen H, Goudsmit J, Biberfeld G, Haverkamp G, Weverling GJ, Lange JM; Ghent Group on HIV in Women and Children. Is there a difference in the efficacy of peripartum antiretroviral regimens in reducing mother-to-child transmission of HIV in Africa? AIDS. 2005 Nov 4;19(16):1865-75. doi: 10.1097/01.aids.0000188423.02786.55.
Results Reference
background
PubMed Identifier
16374215
Citation
McIntyre J. Strategies to prevent mother-to-child transmission of HIV. Curr Opin Infect Dis. 2006 Feb;19(1):33-8. doi: 10.1097/01.qco.0000200290.99790.72.
Results Reference
background
PubMed Identifier
16214193
Citation
Newell ML. Current issues in the prevention of mother-to-child transmission of HIV-1 infection. Trans R Soc Trop Med Hyg. 2006 Jan;100(1):1-5. doi: 10.1016/j.trstmh.2005.05.012. Epub 2005 Oct 7.
Results Reference
background
PubMed Identifier
15249571
Citation
Bulterys M, Jamieson DJ, O'Sullivan MJ, Cohen MH, Maupin R, Nesheim S, Webber MP, Van Dyke R, Wiener J, Branson BM; Mother-Infant Rapid Intervention At Delivery (MIRIAD) Study Group. Rapid HIV-1 testing during labor: a multicenter study. JAMA. 2004 Jul 14;292(2):219-23. doi: 10.1001/jama.292.2.219.
Results Reference
result
PubMed Identifier
14670168
Citation
Jamieson DJ, O'Sullivan MJ, Maupin R, Cohen M, Webber MP, Nesheim S, Lampe M, Garcia P, Lindsay M, Bulterys M. The challenges of informed consent for rapid HIV testing in labor. J Womens Health (Larchmt). 2003 Nov;12(9):889-95. doi: 10.1089/154099903770948113.
Results Reference
result

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Voluntary HIV Counseling, Testing, and Medication for Pregnant Women to Prevent Mother-to-Child HIV Transmission

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