- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT00028145
Prenatal and Postnatal Studies of Interventions for Prevention of Mother-To-Child Transmission
Perinatal Core Protocol
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.
Přehled studie
Postavení
Intervence / Léčba
Detailní popis
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.
Typ studie
Zápis (Aktuální)
Kontakty a umístění
Studijní místa
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San Juan, Portoriko, 00936-5067
- University of Puerto Rico Pediatric HIV/AIDS (6601)
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San Juan, Portoriko, 00936-7344
- San Juan City Hosp. PR NICHD CRS (5031)
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Alabama
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Birmingham, Alabama, Spojené státy, 35233
- Univ. of Alabama Birmingham NICHD CRS (5096)
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Mobile, Alabama, Spojené státy, 36688
- University of South Alabama
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Arizona
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Phoenix, Arizona, Spojené státy, 85006
- Phoenix Childrens Hospital
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California
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Long Beach, California, Spojené státy, 90801
- Long Beach Memorial (Pediatric)
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Long Beach, California, Spojené státy, 90806
- Miller Children's Hospital Long Beach (5093)
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Los Angeles, California, Spojené státy, 900951752
- UCLA Med Ctr / Pediatric
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Los Angeles, California, Spojené státy, 90033
- Usc La Nichd Crs (5048)
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Los Angeles, California, Spojené státy, 90095
- UCLA-Los Angeles/Brazil AIDS Consortium (LABAC) CR (3601)
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Los Angeles, California, Spojené státy, 90033
- Los Angeles County Medical Center/USC
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San Diego, California, Spojené státy, 92103
- Univ of California, San Diego (4601)
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San Francisco, California, Spojené státy, 94117
- Univ. of California San Francisco NICHD CRS (5091)
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Torrance, California, Spojené státy, 90509
- Harbor-UCLA Med Ctr (5045)
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Colorado
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Denver, Colorado, Spojené státy, 80218-1088
- University of Colorado Denver NICHD CRS (5052)
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Connecticut
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Farmington, Connecticut, Spojené státy, 06030-3805
- Connecticut Childrens Medical Center (Pediatric)
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Farmington, Connecticut, Spojené státy, 06030-3805
- University of Connecticut, Farmington
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New Haven, Connecticut, Spojené státy, 06504
- Yale Univ School of Med
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District of Columbia
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Washington, District of Columbia, Spojené státy, 20010-2970
- Children's National Medical Center Washington DC NICHD CRS (5015)
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Washington, District of Columbia, Spojené státy, 200102931
- Washington Hospital Center NICHD CRS (5023)
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Washington, District of Columbia, Spojené státy, 20060
- Howard Univ Hosp (5044)
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Florida
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Fort Lauderdale, Florida, Spojené státy, 33311
- North Broward Hosp District
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Ft Lauderdal, Florida, Spojené státy, 33316
- South Florida CDC Ft Lauderdale NICHD CRS (5055)
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Jacksonville, Florida, Spojené státy, 32209
- University of Florida Jacksonville (5051)
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Miami, Florida, Spojené státy, 33136
- University of Miami Pediatric/Perinatal HIV/AIDS (4201)
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Miami, Florida, Spojené státy, 33136
- Jackson Memorial Hosp
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St Petersburg, Florida, Spojené státy, 33701
- University of South Florida at Tampa (5018)
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Georgia
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Augusta, Georgia, Spojené státy, 30912
- Med College of Georgia
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Columbus, Georgia, Spojené státy, 31901
- The Medical Center
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Illinois
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Chicago, Illinois, Spojené státy, 60612
- Cook County Hospital
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Chicago, Illinois, Spojené státy, 60608
- Mt Sinai Hosp Med Ctr / Dept of Pediatrics
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Chicago, Illinois, Spojené státy, 60612
- Rush University Cook County Hospital NICHD CRS (5083)
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Chicago, Illinois, Spojené státy, 60608-1797
- Womens & Childrens HIV Program
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Chicago, Illinois, Spojené státy, 60612-7234
- Univ of Illinois
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Chicago, Illinois, Spojené státy, 60614
- Chicago Childrens Memorial Hosp (Pediatric)
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Chicago, Illinois, Spojené státy, 60637-1470
- Univ of Chicago Children's Hosp (4001)
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Louisiana
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New Orleans, Louisiana, Spojené státy, 70112-2699
- Tulane University New Orleans (5095)
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New Orleans, Louisiana, Spojené státy, 70112-2699
- Tulane-Lakeside Hospital
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New Orleans, Louisiana, Spojené státy, 70112
- Tulane University Charity Hosp of New Orleans (7201)
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Maryland
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Baltimore, Maryland, Spojené státy, 21287
- Johns Hopkins University NICHD CRS (5092)
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Baltimore, Maryland, Spojené státy, 21201
- University of Maryland Baltimore NICHD CRS (5094)
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Massachusetts
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Boston, Massachusetts, Spojené státy, 02115
- Children's Hospital of Boston NICHD CRS (5009)
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Boston, Massachusetts, Spojené státy, 02118
- Boston Med Ctr (Pediatric) (5011)
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Boston, Massachusetts, Spojené státy, 02478
- Brigham and Women's Hosp
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Springfield, Massachusetts, Spojené státy, 01199
- Baystate Med Ctr of Springfield
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Worcester, Massachusetts, Spojené státy, 01605
- WNE Maternal Pediatric Adolescent AIDS CRS (7301)
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Worcester, Massachusetts, Spojené státy, 01655
- Univ of Massachusetts Med School
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Michigan
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Detroit, Michigan, Spojené státy, 48201-1427
- Hutzel Hospital (5089)
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Detroit, Michigan, Spojené státy, 48201
- Wayne State University Detroit Children's Hosp of Michigan (5041)
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Missouri
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St. Louis, Missouri, Spojené státy, 63108-2138
- St. Louis Children's Hosp
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New Jersey
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Newark, New Jersey, Spojené státy, 07103
- Univ of Med & Dentistry of New Jersey/Univ Hosp
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Newark, New Jersey, Spojené státy, 07103-2714
- Univ of Medicine & Dentistry of New Jersey / Univ Hosp (P2802)
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Newark, New Jersey, Spojené státy, 07103
- New Jersey Medical School (2802)
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New York
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Bronx, New York, Spojené státy, 19461
- Montefiore Medical / AECOM
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Bronx, New York, Spojené státy, 10451
- Lincoln Medical & Mental Health Center
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Bronx, New York, Spojené státy, 10461
- Jacobi Med. Ctr. Bronx NICHD CRS (5013)
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Bronx, New York, Spojené státy, 10457
- Bronx-Lebanon Hospital IMPAACT (6901)
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Brooklyn, New York, Spojené státy, 11203-2098
- Children's Hospital at Downstate
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New York, New York, Spojené státy, 10016
- New York University NY (5012)
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New York, New York, Spojené státy, 10032
- Columbia IMPAACT CRS (4101)
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New York, New York, Spojené státy, 10016
- NYU/Bellevue Hospital
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New York, New York, Spojené státy, 10029
- Metropolitan Hosp Ctr (5003)
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Rochester, New York, Spojené státy, 14642
- Univ of Rochester Med Ctr
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Stony Brook, New York, Spojené státy, 11776
- State Univ of New York at Stony Brook (5040)
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Syracuse, New York, Spojené státy, 13210
- SUNY Upstate Medical Univ
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North Carolina
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Durham, North Carolina, Spojené státy, 27705
- Duke Univ (Pediatric) (DUMC) (4701)
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Oregon
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Portland, Oregon, Spojené státy, 97239
- Oregon Health and Science University
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Pennsylvania
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Philadelphia, Pennsylvania, Spojené státy, 19104
- Hospital of The University of Pennsylvania
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Philadelphia, Pennsylvania, Spojené státy, 19102-1192
- Hahnemann University Hospital (6706)
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Philadelphia, Pennsylvania, Spojené státy, 19134
- The Children's Hospital of Philadelphia (6701)
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Tennessee
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Memphis, Tennessee, Spojené státy, 38105
- St. Jude Childrens Research Hosp, Memphis (6501)
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Memphis, Tennessee, Spojené státy, 38105-2794
- The Regional Med Ctr, Memphis (6502)
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Nashville, Tennessee, Spojené státy, 37232
- Vanderbilt Univ Med Ctr
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Texas
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Houston, Texas, Spojené státy, 77030
- Texas Children's Hosp / Baylor Univ (3801)
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Washington
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Seattle, Washington, Spojené státy, 98105
- Harborview Medical Center NICHD CRS (5027)
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Seattle, Washington, Spojené státy, 98105
- University of Washington NICHD CRS (5029)
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Seattle, Washington, Spojené státy, 98105-0371
- Univ of Washington Children's Hospital Seattle (5017)
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Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
Přijímá zdravé dobrovolníky
Pohlaví způsobilá ke studiu
Metoda odběru vzorků
Studijní populace
Popis
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:
- 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)
Studijní plán
Jak je studie koncipována?
Detaily designu
Kohorty a intervence
Skupina / kohorta |
Intervence / Léčba |
|---|---|
|
1
Pregnant, HIV-infected women
|
Adherence will be assessed using questionnaires at all study visits.
|
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Časové okno |
|---|---|
|
Maternal and infant response to prescribed interventions
Časové okno: Throughout study
|
Throughout study
|
|
Immune and viral parameters of participants taking prescribed interventions
Časové okno: Throughout study
|
Throughout study
|
Sekundární výstupní opatření
Měření výsledku |
Časové okno |
|---|---|
|
Occurrences of genotypic and phenotypic resistance in HIV-infected mothers
Časové okno: Throughout study
|
Throughout study
|
|
Clinical, immunological, and virological responses in HIV-infected women
Časové okno: Throughout study
|
Throughout study
|
|
Mother-to-child transmission rates of resistance mutations
Časové okno: Throughout study
|
Throughout study
|
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Adherence to ART among HIV-infected pregnant women during pregnancy and postpartum
Časové okno: Throughout study
|
Throughout study
|
Spolupracovníci a vyšetřovatelé
Spolupracovníci
Vyšetřovatelé
- Studijní židle: Ruth Tuomala, MD, Director of Obstetrics and Gynecology, Brigham and Women's Hospital
- Studijní židle: Gwen Scott, MD, Pediatric Infectious Diseases, University of Miami School of Medicine
Publikace a užitečné odkazy
Obecné publikace
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia
Primární dokončení (Aktuální)
Dokončení studie (Aktuální)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Odhad)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Odhad)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
Další identifikační čísla studie
- PACTG P1025
- U01AI068632 (Grant/smlouva NIH USA)
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .
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