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CompletedNCT00028145Updated Oct 10, 2014

Prenatal and Postnatal Studies of Interventions for Prevention of Mother-To-Child Transmission

An observational study in HIV Infections and Pregnancy Complications, Infectious, sponsored by International Maternal Pediatric Adolescent AIDS Clinical Trials Group. Completed at 77 sites in 2 countries. Open to female participants aged 14 Years and older. Per ClinicalTrials.gov, last updated 2014-10-10.

Sponsored by International Maternal Pediatric Adolescent AIDS Clinical Trials Group · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
3,090
Ages
14 Years and older
Sex
Female
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Study summary

The purpose of this study is to collect and study clinical and laboratory information about a pregnant or new mother and her medical care that will increase our knowledge of the best care for HIV-infected pregnant women and their children.

The rate of transmission of HIV from mothers to their infants has gone down. Specific U.S. Public Health Service guidelines recommend that HIV-infected pregnant women be treated with anti-HIV therapies; but the effectiveness of treatment and safety for the mother and her infant have not been fully examined. This study will monitor the health of women and their infants while they receive anti-HIV therapy. Also, this study will provide information that may be used for future studies.

Read the detailed description

The current low rate of vertical transmission of HIV in the U.S. limits the number and types of questions concerning transmission risk and pathogenesis that can be addressed by a single clinical trial. Specific U.S. Public Health Service guidelines recommend antiretroviral therapy (ART) during pregnancy to maximize health of women. However, data regarding the effectiveness and safety of and adherence to ART during pregnancy are limited. It is both appropriate and necessary for theInternational Maternal Pediatric Adolescent AIDS Clinical Trials Group (IMPAACT) to recruit pregnant women into a non-interventional, analytic, epidemiologic study to methodically collect clinical and laboratory data from them and their infants. This way, the IMPAACT can achieve the aims of evaluating management of HIV-infected women during pregnancy and determining the safety and effectiveness of ART and other interventions intended to prevent vertical transmission and/or improve maternal health. In addition, longitudinally collected core protocol data and repository specimens will enable future substudies.

Participants receive no protocol specific treatment or other intervention as part of this study. The study involves the follow-up of HIV-infected women enrolled during pregnancy or at the time of delivery for 6 months postpartum and their infants for the first 6 months of life. There will be 8 study visits for enrolled participants and 6 study visits for infants. Data concerning ART use, adherence to medications, and review of symptoms relevant to side effects and toxicities are collected through administration of questionnaires at all maternal visits. Phlebotomy is conducted to obtain specimens for a repository and for required laboratory tests. During labor and delivery, maternal blood is obtained for lymphocyte subset and viral load assays and for repository storage. Collection of amniotic fluid at the time of cesarean section is encouraged. These collections are submitted to a central repository. Data for the core protocol are abstracted from the infant's medical record at the time of birth and at each postnatal visit.

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Conditions studied

  • HIV Infections
  • Pregnancy Complications, Infectious

Keywords

  • Women's Health
  • Disease Transmission, Vertical
  • Preventive Medicine
  • Treatment Experienced
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In context

HIV Infections

4,342 studies on the registry are indexed under HIV Infections; 240 are open to participants now.

This study's enrollment of 3,090 is above the median of 200 across 731 observational studies indexed under HIV Infections.

Browse HIV Infections studies →

Lead sponsor

International Maternal Pediatric Adolescent AIDS Clinical Trials Group is the lead sponsor of 27 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
14 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Primary care clinics

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • HIV infected
  • At least 14 weeks pregnant OR have delivered a liveborn or stillborn infant and are within 14 days of the delivery
  • Currently receiving care at an IMPAACT or other participating site
  • Have a parent or guardian willing to provide signed informed consent, if applicable
  • Mentally capable of giving informed consent to have the infant and self followed at an IMPAACT site

Exclusion criteria

Exclusion Criteria:

  • Intend to end the pregnancy
  • Unable to come for a study visit within 14 days after delivery (if known to be HIV infected prior to delivery) OR within 28 days after delivery (if found to be HIV infected at the time of labor and delivery or within 14 days after delivery)
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
3,090 participants (actual)
Biospecimen retention
Samples with dna

Groups and cohorts

  • 1

    Pregnant, HIV-infected women

    Behavioral: Adherence assessment

Interventions

  • BehavioralAdherence assessment

    Adherence will be assessed using questionnaires at all study visits.

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What researchers measure

Primary outcomes

  1. Maternal and infant response to prescribed interventions

    Time frame: Throughout study

  2. Immune and viral parameters of participants taking prescribed interventions

    Time frame: Throughout study

Secondary outcomes

  1. Occurrences of genotypic and phenotypic resistance in HIV-infected mothers

    Time frame: Throughout study

  2. Clinical, immunological, and virological responses in HIV-infected women

    Time frame: Throughout study

  3. Mother-to-child transmission rates of resistance mutations

    Time frame: Throughout study

  4. Adherence to ART among HIV-infected pregnant women during pregnancy and postpartum

    Time frame: Throughout study

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Study locations

77 sites
  • Univ. of Alabama Birmingham NICHD CRS (5096)
    Birmingham, Alabama 35233, United States
  • University of South Alabama
    Mobile, Alabama 36688, United States
  • Phoenix Childrens Hospital
    Phoenix, Arizona 85006, United States
  • Long Beach Memorial (Pediatric)
    Long Beach, California 90801, United States
  • Miller Children's Hospital Long Beach (5093)
    Long Beach, California 90806, United States
  • Los Angeles County Medical Center/USC
    Los Angeles, California 90033, United States
  • Usc La Nichd Crs (5048)
    Los Angeles, California 90033, United States
  • UCLA Med Ctr / Pediatric
    Los Angeles, California 900951752, United States
  • UCLA-Los Angeles/Brazil AIDS Consortium (LABAC) CR (3601)
    Los Angeles, California 90095, United States
  • Univ of California, San Diego (4601)
    San Diego, California 92103, United States
  • Univ. of California San Francisco NICHD CRS (5091)
    San Francisco, California 94117, United States
  • Harbor-UCLA Med Ctr (5045)
    Torrance, California 90509, United States
  • University of Colorado Denver NICHD CRS (5052)
    Denver, Colorado 80218-1088, United States
  • Connecticut Childrens Medical Center (Pediatric)
    Farmington, Connecticut 06030-3805, United States
  • University of Connecticut, Farmington
    Farmington, Connecticut 06030-3805, United States
  • Yale Univ School of Med
    New Haven, Connecticut 06504, United States
  • Children's National Medical Center Washington DC NICHD CRS (5015)
    Washington D.C., District of Columbia 20010-2970, United States
  • Washington Hospital Center NICHD CRS (5023)
    Washington D.C., District of Columbia 200102931, United States
  • Howard Univ Hosp (5044)
    Washington D.C., District of Columbia 20060, United States
  • North Broward Hosp District
    Fort Lauderdale, Florida 33311, United States
  • South Florida CDC Ft Lauderdale NICHD CRS (5055)
    Fort Lauderdal, Florida 33316, United States
  • University of Florida Jacksonville (5051)
    Jacksonville, Florida 32209, United States
  • Jackson Memorial Hosp
    Miami, Florida 33136, United States
  • University of Miami Pediatric/Perinatal HIV/AIDS (4201)
    Miami, Florida 33136, United States
  • University of South Florida at Tampa (5018)
    St. Petersburg, Florida 33701, United States
  • Med College of Georgia
    Augusta, Georgia 30912, United States
  • The Medical Center
    Columbus, Georgia 31901, United States
  • Womens & Childrens HIV Program
    Chicago, Illinois 60608-1797, United States
  • Mt Sinai Hosp Med Ctr / Dept of Pediatrics
    Chicago, Illinois 60608, United States
  • Univ of Illinois
    Chicago, Illinois 60612-7234, United States
  • Cook County Hospital
    Chicago, Illinois 60612, United States
  • Rush University Cook County Hospital NICHD CRS (5083)
    Chicago, Illinois 60612, United States
  • Chicago Childrens Memorial Hosp (Pediatric)
    Chicago, Illinois 60614, United States
  • Univ of Chicago Children's Hosp (4001)
    Chicago, Illinois 60637-1470, United States
  • Tulane University New Orleans (5095)
    New Orleans, Louisiana 70112-2699, United States
  • Tulane-Lakeside Hospital
    New Orleans, Louisiana 70112-2699, United States
  • Tulane University Charity Hosp of New Orleans (7201)
    New Orleans, Louisiana 70112, United States
  • University of Maryland Baltimore NICHD CRS (5094)
    Baltimore, Maryland 21201, United States
  • Johns Hopkins University NICHD CRS (5092)
    Baltimore, Maryland 21287, United States
  • Children's Hospital of Boston NICHD CRS (5009)
    Boston, Massachusetts 02115, United States
  • Boston Med Ctr (Pediatric) (5011)
    Boston, Massachusetts 02118, United States
  • Brigham and Women's Hosp
    Boston, Massachusetts 02478, United States
  • Baystate Med Ctr of Springfield
    Springfield, Massachusetts 01199, United States
  • WNE Maternal Pediatric Adolescent AIDS CRS (7301)
    Worcester, Massachusetts 01605, United States
  • Univ of Massachusetts Med School
    Worcester, Massachusetts 01655, United States
  • Hutzel Hospital (5089)
    Detroit, Michigan 48201-1427, United States
  • Wayne State University Detroit Children's Hosp of Michigan (5041)
    Detroit, Michigan 48201, United States
  • St. Louis Children's Hosp
    St Louis, Missouri 63108-2138, United States
  • Univ of Medicine & Dentistry of New Jersey / Univ Hosp (P2802)
    Newark, New Jersey 07103-2714, United States
  • New Jersey Medical School (2802)
    Newark, New Jersey 07103, United States
  • Univ of Med & Dentistry of New Jersey/Univ Hosp
    Newark, New Jersey 07103, United States
  • Children's Hospital at Downstate
    Brooklyn, New York 11203-2098, United States
  • New York University NY (5012)
    New York, New York 10016, United States
  • NYU/Bellevue Hospital
    New York, New York 10016, United States
  • Metropolitan Hosp Ctr (5003)
    New York, New York 10029, United States
  • Columbia IMPAACT CRS (4101)
    New York, New York 10032, United States
  • Univ of Rochester Med Ctr
    Rochester, New York 14642, United States
  • State Univ of New York at Stony Brook (5040)
    Stony Brook, New York 11776, United States
  • SUNY Upstate Medical Univ
    Syracuse, New York 13210, United States
  • Lincoln Medical & Mental Health Center
    The Bronx, New York 10451, United States
  • Bronx-Lebanon Hospital IMPAACT (6901)
    The Bronx, New York 10457, United States
  • Jacobi Med. Ctr. Bronx NICHD CRS (5013)
    The Bronx, New York 10461, United States
  • Montefiore Medical / AECOM
    The Bronx, New York 19461, United States
  • Duke Univ (Pediatric) (DUMC) (4701)
    Durham, North Carolina 27705, United States
  • Oregon Health and Science University
    Portland, Oregon 97239, United States
  • Hahnemann University Hospital (6706)
    Philadelphia, Pennsylvania 19102-1192, United States
  • Hospital of the University of Pennsylvania
    Philadelphia, Pennsylvania 19104, United States
  • The Children's Hospital of Philadelphia (6701)
    Philadelphia, Pennsylvania 19134, United States
  • The Regional Med Ctr, Memphis (6502)
    Memphis, Tennessee 38105-2794, United States
  • St. Jude Childrens Research Hosp, Memphis (6501)
    Memphis, Tennessee 38105, United States
  • Vanderbilt Univ Med Ctr
    Nashville, Tennessee 37232, United States
  • Texas Children's Hosp / Baylor Univ (3801)
    Houston, Texas 77030, United States
  • Univ of Washington Children's Hospital Seattle (5017)
    Seattle, Washington 98105-0371, United States
  • Harborview Medical Center NICHD CRS (5027)
    Seattle, Washington 98105, United States
  • University of Washington NICHD CRS (5029)
    Seattle, Washington 98105, United States
  • University of Puerto Rico Pediatric HIV/AIDS (6601)
    San Juan, 00936-5067, Puerto Rico
  • San Juan City Hosp. PR NICHD CRS (5031)
    San Juan, 00936-7344, Puerto Rico
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References and documents

Publications

  • Ciambrone D, Loewenthal HG, Bazerman LB, Zorilla C, Urbina B, Mitty JA. Adherence among women with HIV infection in Puerto Rico: the potential use of modified directly observed therapy (MDOT) among pregnant and postpartum women. Women Health. 2006;44(4):61-77. doi: 10.1300/j013v44n04_04. PubMed 17456464 ↗
  • Kingston MA, Letham CJ, McQuillan O. Adherence to antiretroviral therapy in pregnancy. Int J STD AIDS. 2007 Nov;18(11):787-9. doi: 10.1258/095646207782212216. PubMed 18005515 ↗
  • Bardeguez AD, Lindsey JC, Shannon M, Tuomala RE, Cohn SE, Smith E, Stek A, Buschur S, Cotter A, Bettica L, Read JS; PACTG 1025 Protocol Team. Adherence to antiretrovirals among US women during and after pregnancy. J Acquir Immune Defic Syndr. 2008 Aug 1;48(4):408-17. doi: 10.1097/QAI.0b013e31817bbe80. PubMed 18614923 ↗
  • Momplaisir F, Hussein M, Kacanek D, Brady K, Agwu A, Scott G, Tuomala R, Bennett D. Perinatal Depressive Symptoms, Human Immunodeficiency Virus (HIV) Suppression, and the Underlying Role of Antiretroviral Therapy Adherence: A Longitudinal Mediation Analysis in the IMPAACT P1025 Cohort. Clin Infect Dis. 2021 Oct 20;73(8):1379-1387. doi: 10.1093/cid/ciab416. PubMed 33982083 ↗
  • Jao J, Kacanek D, Williams PL, Geffner ME, Livingston EG, Sperling RS, Patel K, Bardeguez AD, Burchett SK, Chakhtoura N, Scott GB, Van Dyke RB, Abrams EJ; Pediatric HIV/AIDS Cohort Study and the International Maternal Pediatric Adolescent AIDS Clinical Trials P1025 Protocol; Pediatric HIV/AIDS Cohort Study and the International Maternal Pediatric Adolescent AIDS Clinical Trials P1025 Protocol. Birth Weight and Preterm Delivery Outcomes of Perinatally vs Nonperinatally Human Immunodeficiency Virus-Infected Pregnant Women in the United States: Results From the PHACS SMARTT Study and IMPAACT P1025 Protocol. Clin Infect Dis. 2017 Sep 15;65(6):982-989. doi: 10.1093/cid/cix488. PubMed 28575201 ↗
  • Scott GB, Brogly SB, Muenz D, Stek AM, Read JS; International Maternal Pediatric Adolescent AIDS Clinical Trials Group (IMPAACT) P1025 Study Team. Missed Opportunities for Prevention of Mother-to-Child Transmission of Human Immunodeficiency Virus. Obstet Gynecol. 2017 Apr;129(4):621-628. doi: 10.1097/AOG.0000000000001929. PubMed 28277349 ↗
  • Livingston EG, Huo Y, Patel K, Tuomala RE, Scott GB, Stek A; P1025 Team of the International Maternal Pediatric Adolescent AIDS Clinical Trials (IMPAACT) Group. Complications and Route of Delivery in a Large Cohort Study of HIV-1-Infected Women-IMPAACT P1025. J Acquir Immune Defic Syndr. 2016 Sep 1;73(1):74-82. doi: 10.1097/QAI.0000000000001021. PubMed 27082506 ↗
  • Katz IT, Leister E, Kacanek D, Hughes MD, Bardeguez A, Livingston E, Stek A, Shapiro DE, Tuomala R. Factors associated with lack of viral suppression at delivery among highly active antiretroviral therapy-naive women with HIV: a cohort study. Ann Intern Med. 2015 Jan 20;162(2):90-9. doi: 10.7326/M13-2005. PubMed 25599347 ↗
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Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Oct 2002, a primary completion of Jun 2013 and a completion of Jun 2013. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 13, 2001
First posted
Dec 14, 2001
Start
Oct 2002
Primary completionActual
Jun 2013
CompletionActual
Jun 2013
Last update
Oct 10, 2014
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Oct 10, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00028145
Lead sponsor
International Maternal Pediatric Adolescent AIDS Clinical Trials Group
Responsible party
Sponsor
First posted
Dec 14, 2001
Start date
Oct 2002
Primary completion
Jun 2013
Completion
Jun 2013
Last update
Oct 10, 2014

Study contacts

Ruth Tuomala, MD
study chair · Director of Obstetrics and Gynecology, Brigham and Women's Hospital
Gwen Scott, MD
study chair · Pediatric Infectious Diseases, University of Miami School of Medicine

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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