- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT00000828
Study of Perinatal Transmission of Zidovudine-Resistant HIV Among Pregnant Women Treated With Zidovudine
To identify patterns of zidovudine ( AZT ) susceptibility among mother/infant pairs with perinatal HIV transmission.
Most HIV-infected infants acquire their disease via perinatal transmission. Since transmission of HIV-resistant strains to infants could alter the course of disease and response to currently recommended treatment, a study to assess the patterns of AZT susceptibility among mother/infant pairs with perinatal transmission is essential to delineate future therapeutic strategies.
Panoramica dello studio
Stato
Condizioni
Descrizione dettagliata
Most HIV-infected infants acquire their disease via perinatal transmission. Since transmission of HIV-resistant strains to infants could alter the course of disease and response to currently recommended treatment, a study to assess the patterns of AZT susceptibility among mother/infant pairs with perinatal transmission is essential to delineate future therapeutic strategies.
HIV-infected pregnant women are enrolled at 20-36 weeks gestation. Patients have blood drawn for HIV culture at study entry and at delivery. Infants have blood drawn for HIV culture at delivery and at 1, 3, 6, and 18 months of age.
Tipo di studio
Iscrizione
Contatti e Sedi
Luoghi di studio
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San Juan, Porto Rico, 009367344
- San Juan City Hosp
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Alabama
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Birmingham, Alabama, Stati Uniti, 35294
- Univ of Alabama at Birmingham Schl of Med / Pediatrics
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California
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La Jolla, California, Stati Uniti, 920930672
- UCSD Med Ctr / Pediatrics / Clinical Sciences
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Long Beach, California, Stati Uniti, 90801
- Long Beach Memorial (Pediatric)
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Los Angeles, California, Stati Uniti, 90033
- Los Angeles County - USC Med Ctr
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Los Angeles, California, Stati Uniti, 905022004
- Harbor - UCLA Med Ctr / UCLA School of Medicine
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Los Angeles, California, Stati Uniti, 900951752
- UCLA Med Ctr / Pediatric
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Connecticut
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Farmington, Connecticut, Stati Uniti, 06032
- Univ of Connecticut / Farmington
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Hartford, Connecticut, Stati Uniti, 06106
- Connecticut Children's Med Ctr - Pediatric
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District of Columbia
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Washington, District of Columbia, Stati Uniti, 200102916
- Children's Hosp of Washington DC
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Washington, District of Columbia, Stati Uniti, 20060
- Howard Univ Hosp
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Florida
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Miami, Florida, Stati Uniti, 33161
- Univ of Miami (Pediatric)
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Illinois
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Chicago, Illinois, Stati Uniti, 606371470
- Univ of Chicago Children's Hosp
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Louisiana
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New Orleans, Louisiana, Stati Uniti, 701122699
- Tulane Univ / Charity Hosp of New Orleans
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New Orleans, Louisiana, Stati Uniti, 70112
- Univ Hosp
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Maryland
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Baltimore, Maryland, Stati Uniti, 212874933
- Johns Hopkins Hosp - Pediatric
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Massachusetts
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Boston, Massachusetts, Stati Uniti, 02115
- Brigham and Women's Hosp
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Boston, Massachusetts, Stati Uniti, 021155724
- Children's Hosp of Boston
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Springfield, Massachusetts, Stati Uniti, 01199
- Baystate Med Ctr of Springfield
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New Jersey
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Newark, New Jersey, Stati Uniti, 071032714
- Univ of Medicine & Dentistry of New Jersey / Univ Hosp
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New York
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Bronx, New York, Stati Uniti, 10457
- Bronx Lebanon Hosp Ctr
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New York, New York, Stati Uniti, 10016
- Bellevue Hosp / New York Univ Med Ctr
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New York, New York, Stati Uniti, 10032
- Columbia Presbyterian Med Ctr
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New York, New York, Stati Uniti, 10032
- Incarnation Children's Ctr / Columbia Presbyterian Med Ctr
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New York, New York, Stati Uniti, 10029
- Mount Sinai Med Ctr / Pediatrics
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Rochester, New York, Stati Uniti, 14642
- Univ of Rochester Medical Center
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Syracuse, New York, Stati Uniti, 13210
- SUNY Health Sciences Ctr at Syracuse / Pediatrics
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North Carolina
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Durham, North Carolina, Stati Uniti, 277103499
- Duke Univ Med Ctr
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Ohio
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Columbus, Ohio, Stati Uniti, 432052696
- Columbus Children's Hosp
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria
Prior Medication: Required:
- At least 6 months of prior AZT, including continuously during the current pregnancy.
Patients must have:
- HIV seropositivity.
- CD4 count <= 300 cells/mm3.
- Gestational age of 20-36 weeks, with intention to carry pregnancy to term.
- At least 6 months of prior AZT therapy, including continuous AZT therapy during the current pregnancy.
Exclusion Criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
- Evidence of pre-existing fetal anomalies that would preclude survival to the end of the study, such as anencephaly, renal agenesis, or Potter's syndrome.
Concurrent Medication:
Excluded:
- Antiretrovirals other than AZT.
Piano di studio
Come è strutturato lo studio?
Collaboratori e investigatori
Investigatori
- Cattedra di studio: Bardeguez AD
- Cattedra di studio: Pitt J
Pubblicazioni e link utili
Pubblicazioni generali
- Garcia PM, Kalish LA, Pitt J, Minkoff H, Quinn TC, Burchett SK, Kornegay J, Jackson B, Moye J, Hanson C, Zorrilla C, Lew JF. Maternal levels of plasma human immunodeficiency virus type 1 RNA and the risk of perinatal transmission. Women and Infants Transmission Study Group. N Engl J Med. 1999 Aug 5;341(6):394-402. doi: 10.1056/NEJM199908053410602.
- Bardeguez AD. Management of HIV infection for the childbearing age woman. Clin Obstet Gynecol. 1996 Jun;39(2):344-60. doi: 10.1097/00003081-199606000-00009. No abstract available.
- Bardeguez AD, Taylor U, Appuzio J, Leus C, Lister M, Denny T, Palumbo P, Connor E. Characteristics of pregnant women infected with human immunodeficiency virus 1: Newark perinatal transmission study. Int Conf AIDS. 1991 Jun 16-21;7(2):193 (abstract no WB2044)
- Welles SL, Pitt J, Colgrove R, McIntosh K, Chung PH, Colson A, Lockman S, Fowler MG, Hanson C, Landesman S, Moye J, Rich KC, Zorrilla C, Japour AJ. HIV-1 genotypic zidovudine drug resistance and the risk of maternal--infant transmission in the women and infants transmission study. The Women and Infants Transmission Study Group. AIDS. 2000 Feb 18;14(3):263-71. doi: 10.1097/00002030-200002180-00008.
Studiare le date dei record
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Infezioni da virus a RNA
- Malattie virali
- Infezioni
- Infezioni a trasmissione ematica
- Malattie trasmissibili
- Malattie sessualmente trasmissibili, virali
- Malattie trasmesse sessualmente
- Infezioni da lentivirus
- Infezioni da retroviridae
- Sindromi da deficit immunologico
- Malattie del sistema immunitario
- Infezioni da HIV
Altri numeri di identificazione dello studio
- ACTG 255
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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