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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00000828
Other study ID # ACTG 255
Secondary ID
Status Completed
Phase N/A
First received November 2, 1999
Last updated June 23, 2005

Study information

Verified date October 1997
Source National Institute of Allergy and Infectious Diseases (NIAID)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 250
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Female
Age group 13 Years to 60 Years
Eligibility 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.

Study Design

N/A


Related Conditions & MeSH terms


Locations

Country Name City State
Puerto Rico San Juan City Hosp San Juan
United States Johns Hopkins Hosp - Pediatric Baltimore Maryland
United States Univ of Alabama at Birmingham Schl of Med / Pediatrics Birmingham Alabama
United States Brigham and Women's Hosp Boston Massachusetts
United States Children's Hosp of Boston Boston Massachusetts
United States Bronx Lebanon Hosp Ctr Bronx New York
United States Univ of Chicago Children's Hosp Chicago Illinois
United States Columbus Children's Hosp Columbus Ohio
United States Duke Univ Med Ctr Durham North Carolina
United States Univ of Connecticut / Farmington Farmington Connecticut
United States Connecticut Children's Med Ctr - Pediatric Hartford Connecticut
United States UCSD Med Ctr / Pediatrics / Clinical Sciences La Jolla California
United States Long Beach Memorial (Pediatric) Long Beach California
United States Harbor - UCLA Med Ctr / UCLA School of Medicine Los Angeles California
United States Los Angeles County - USC Med Ctr Los Angeles California
United States UCLA Med Ctr / Pediatric Los Angeles California
United States Univ of Miami (Pediatric) Miami Florida
United States Tulane Univ / Charity Hosp of New Orleans New Orleans Louisiana
United States Univ Hosp New Orleans Louisiana
United States Bellevue Hosp / New York Univ Med Ctr New York New York
United States Columbia Presbyterian Med Ctr New York New York
United States Incarnation Children's Ctr / Columbia Presbyterian Med Ctr New York New York
United States Mount Sinai Med Ctr / Pediatrics New York New York
United States Univ of Medicine & Dentistry of New Jersey / Univ Hosp Newark New Jersey
United States Univ of Rochester Medical Center Rochester New York
United States Baystate Med Ctr of Springfield Springfield Massachusetts
United States SUNY Health Sciences Ctr at Syracuse / Pediatrics Syracuse New York
United States Children's Hosp of Washington DC Washington District of Columbia
United States Howard Univ Hosp Washington District of Columbia

Sponsors (1)

Lead Sponsor Collaborator
National Institute of Allergy and Infectious Diseases (NIAID)

Countries where clinical trial is conducted

United States,  Puerto Rico, 

References & Publications (4)

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)

Bardeguez AD. Management of HIV infection for the childbearing age woman. Clin Obstet Gynecol. 1996 Jun;39(2):344-60. Review. — View Citation

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. — View Citation

Japour AJ, Welles S, McIntosh K, Colson A, Chung P, Lockman S, Davenny K, Fowler MG, Hansen IC, Kalish L, Moye J, Rick K, Zorilla C, Pitt J. ZDV resistance (ZDVR) mutations in ZDV exposed mother infant pairs: preliminary findings from the women and infants transmission study (WITS). Int Conf AIDS. 1996 Jul 7-12;11(1):370 (abstract no TuC2606)

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