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Antibiotics to Reduce Chorioamnionitis-Related Perinatal HIV Transmission

This study has been completed.

Sponsors and Collaborators: National Institute of Child Health and Human Development (NICHD)
National Institute of Allergy and Infectious Diseases (NIAID)
National Institute of Mental Health (NIMH)
National Institute on Drug Abuse (NIDA)
Information provided by: National Institute of Allergy and Infectious Diseases (NIAID)
ClinicalTrials.gov Identifier: NCT00021671
  Purpose

The purpose of this study is to see if antibiotic drugs given to treat an infection of the uterus during pregnancy can reduce the chances of HIV being passed from an HIV-positive mother to her baby.

A link between bacterial disease of the vagina, premature birth, infection of the uterus during pregnancy, and the passing of HIV from a mother to her baby has been found. Early treatment of these problems may reduce the risk of passing HIV from an HIV-positive mother to her baby.

[Note: As of 02/21/03, enrollment into this study was halted because preliminary data showed that the study antibiotics were not effective in preventing mother-to-child HIV transmission.]


Condition Intervention Phase
HIV Infections
Drug: Erythromycin
Drug: Nevirapine
Drug: Ampicillin sodium
Drug: Metronidazole
Phase III

MedlinePlus related topics:   AIDS    AIDS and Pregnancy    Antibiotics   

ChemIDplus related topics:   Nevirapine    Metronidazole    Metronidazole hydrochloride    Metronidazole phosphate    Erythromycin    Erythromycin estolate    Erythromycin ethylsuccinate    Erythromycin Gluceptate    Erythromycin stearate    Ampicillin    Ampicillin sodium    Ampicillin trihydrate   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Prevention, Double-Blind, Efficacy Study
Official Title:   Phase III Trial of Antibiotics to Reduce Chorioamnionitis-Related Perinatal HIV Transmission

Further study details as provided by National Institute of Allergy and Infectious Diseases (NIAID):

Estimated Enrollment:   3720

Detailed Description:

Obstetric risk factors for HIV maternal-child transmission (MCT) include preterm birth, prolonged rupture of the membranes, and chorioamnionitis. Many preterm births are associated with and likely caused by chorioamnionitis. The relationship between bacterial vaginosis, preterm birth, histologic chorioamnionitis, and perinatal transmission of HIV has been consistently demonstrated. Perinatal HIV transmission is more common in preterm infants, and there is now evidence that subclinical chorioamnionitis is a substantial risk factor for MCT. For this study, the primary hypothesis is that early and appropriate treatment of subclinical chorioamnionitis prior to the onset of spontaneous preterm labor, and/or antibiotic treatment during labor, to prevent premature rupture of membrane-associated-chorioamnionitis, will reduce the risk of perinatal HIV transmission.

[Note: As of 02/21/03, enrollment into this study was halted because preliminary data showed that the study antibiotics were not effective in preventing mother-to-child HIV transmission.]

At 20 to 24 weeks, women who are randomized to receive antibiotics receive metronidazole and erythromycin for 7 days. Women randomized to the control group receive identically appearing placebos. With the onset of contractions and/or premature rupture of membranes, study participants will initiate a second oral course of antibiotics consisting of metronidazole and ampicillin or placebo every 4 hours, continuing after delivery until the course is completed. All HIV-infected women and their neonates will be offered the HIVNET 012 nevirapine (NVP) regimen. If the mother accepts the NVP for herself and her baby, she will be given 1 dose of NVP to be taken at onset of labor, and her baby will receive 1 dose of NVP at 72 hours post-birth or discharge, whichever occurs earlier. If the mother refuses NVP or is uninfected, she will receive a matched placebo at the 26- to 30-week visit to preserve participant confidentiality. This study takes place in Blantyre and Lilongwe, Malawi, in Lusaka, Zambia, and in Dar es Salaam, Tanzania.

  Eligibility
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria

  • HIV positive.
  • 20 to 24 weeks pregnant.
  • Willing to take the planned antibiotic treatment.
  • Planning to deliver at 1 of the study sites.
  • Willing to come back for follow-up visits for 1 year after the baby is born.

Exclusion Criteria

  • Have taken antibiotics, except for syphilis or gonorrhea, within the last 2 weeks.
  • Are allergic to penicillin, ampicillin, erythromycin, or metronidazole.
  • Have major illnesses, such as diabetes, severe kidney or heart disease, or active tuberculosis, which might affect the pregnancy.
  • Are having major problems with the pregnancy, such as placenta previa, ruptured membranes, or multiple pregnancy.
  • Have a central nervous system disease, such as seizures.
  • Are taking anticoagulant drugs.
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00021671

Locations
United States, North Carolina
Megan Valentine    
      Research Triangle Park, North Carolina, United States, 27709

Sponsors and Collaborators

Investigators
Study Chair:     Taha E Taha, MD, PhD     Johns Hopkins University    
Study Chair:     Robert Goldenberg, MD     Department of Obstetrics and Gynecology, University of Alabama at Birmingham    
  More Information


Click here for more information about nevirapine  This link exits the ClinicalTrials.gov site
 
Click here for more information about HIV and pregnancy  This link exits the ClinicalTrials.gov site
 
Click here for more information on medication regimens for HIV positive pregnant women  This link exits the ClinicalTrials.gov site
 
Click here for more information on after birth care for HIV positive women and their babies  This link exits the ClinicalTrials.gov site
 
Haga clic aquí para ver información sobre este ensayo clínico en español.  This link exits the ClinicalTrials.gov site
 

Publications of Results:

Other Publications:

Publications indexed to this study:

Study ID Numbers:   HIVNET 024
First Received:   July 31, 2001
Last Updated:   July 31, 2008
ClinicalTrials.gov Identifier:   NCT00021671
Health Authority:   United States: Federal Government

Keywords provided by National Institute of Allergy and Infectious Diseases (NIAID):
Drug Therapy, Combination  
Ampicillin  
Nevirapine  
Disease Transmission, Vertical  
Anti-Infective Agents  
Erythromycin  
Reverse Transcriptase Inhibitors
Metronidazole
Anti-HIV Agents
Chorioamnionitis
HIV Seronegativity

Study placed in the following topic categories:
Erythromycin stearate
Metronidazole
Sexually Transmitted Diseases, Viral
Pregnancy Complications
Erythromycin Ethylsuccinate
Acquired Immunodeficiency Syndrome
Obstetric Labor Complications
Ampicillin
Rupture
Erythromycin
Fetal Membranes, Premature Rupture
Immunologic Deficiency Syndromes
Virus Diseases
Nevirapine
Fetal Diseases
Erythromycin Estolate
HIV Infections
Sexually Transmitted Diseases
Chorioamnionitis
Retroviridae Infections

Additional relevant MeSH terms:
Placenta Diseases
Anti-Infective Agents
Antiprotozoal Agents
RNA Virus Infections
Anti-HIV Agents
Slow Virus Diseases
Molecular Mechanisms of Pharmacological Action
Immune System Diseases
Physiological Effects of Drugs
Gastrointestinal Agents
Enzyme Inhibitors
Infection
Antiviral Agents
Pharmacologic Actions
Reverse Transcriptase Inhibitors
Anti-Bacterial Agents
Protein Synthesis Inhibitors
Antiparasitic Agents
Anti-Retroviral Agents
Radiation-Sensitizing Agents
Therapeutic Uses
Lentivirus Infections
Nucleic Acid Synthesis Inhibitors

ClinicalTrials.gov processed this record on October 10, 2008




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