Skip to main content
OpenTrials
Completed

NCT Number: NCT00339612

NISDI Pediatric Latin American Countries Epidemiologic Study (PLACES): A Prospective Observational Study of HIV-Infected Children at Clinical Sites in Latin American Countries

This is an observational, prospective cohort study to describe the demographic, clinical, immunologic, and virologic characteristics of HIV-infected children at participating clinical sites in Latin American countries. Enrollment in this study will consist of approximately 500 HIV-infected children in two cohorts who acquired HIV infection through mother-to-child transmission (MTCT). The first group will be a static cohort consisting of HIV-infected children who were five years of age or younger when previously enrolled into the NISDI Pediatric Protocol. The second cohort will be a dynamic cohort of prospectively enrolled, HIV-infected children who are five years of age or younger. We will characterize complications from both the disease and its treatments. Subjects will be evaluated every six months for approximately five years and assessments of growth, morbidity, disease progression and mortality will be made.

Completed

Looking for future studies?

Notify Me

Key information

Age range

Up to 21 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Universidade Federal de Minas Gerais, Belo Horizonte, Brazil

Loading trial locations.

About this study

This is an observational, prospective cohort study to describe the demographic, clinical, immunologic, and virologic characteristics of HIV-infected children at participating clinical sites in Latin American countries. Enrollment in this study will consist of approximately 500 HIV-infected children in two cohorts who acquired HIV infection through mother-to-child transmission (MTCT). The first group will be a static cohort consisting of HIV-infected children who were five years of age or younger when previously enrolled into the NISDI Pediatric Protocol. The second cohort will be a dynamic cohort of prospectively enrolled, HIV-infected children who are five years of age or younger. We will characterize complications from both the disease and its treatments. Subjects will be evaluated every six months for approximately five years and assessments of growth, morbidity, disease progression and mortality will be made.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

  • INCLUSION CRITERIA:

Static Cohort:

  • Previous participation in a NISDI Protocol
  • Less then 6 years of age (before their 6th birthday) at the time of enrollment into the NISDI Pediatric Protocol
  • HIV-infected
  • HIV infection must be documented in the medical records by:
  • For children less than 18 months old when tested, two or more of the following (separate determinations on separate blood specimens):
  • Positive HIV culture
  • Positive HIV DNA PCR
  • Positive neutralizable p24 antigen
  • Quantitative HIV RNA greater than or equal to 10,000 copies/ml
  • For children greater than or equal to 18 months old when tested, two or more of the following (separate determinations on separate blood specimens):
  • Reactive test for HIV antibody in a sample obtained at greater than or equal to 15 months of age with confirmatory test by Western Blot or Immunofluorescence assay
  • Positive HIV culture
  • Positive HIV DNA PCR
  • Positive neutralizable p24 antigen
  • Quantitative HIV RNA greater than or equal to 1,000 copies/ml
  • Documentation of maternal HIV infection by country appropriate National Guidelines
  • Signed informed consent from parent or legal guardian. An informed assent document will be provided for children 8 years of age or older when appropriate.
  • Subjects must be able to be followed at a participating clinical site.
  • Subjects may be co-enrolled in clinical trials for treatment of HIV infection, opportunistic infections, or other HIV-related effects.

Dynamic cohort:

  • HIV-infected less then 6 years of age (before their 6th birthday) at enrollment into this protocol
  • HIV infection documented by:
  • For children <18 months old when tested, two or more of the following (separate determinations on separate blood specimens):
  • Positive HIV culture
  • Positive HIV DNA PCR
  • Positive neutralizable p24 antigen
  • Quantitative HIV RNA greater than or equal to 10,000 copies/ml
  • For children greater than or equal to 18 months old when tested, two or more of the following (separate determinations on separate blood specimens):
  • Reactive test for HIV antibody in a sample obtained at greater than or equal to 15 months of age with confirmatory test by Western Blot or Immunofluorescence assay
  • Positive HIV culture
  • Positive HIV DNA PCR
  • Positive neutralizable p24 antigen
  • Quantitative HIV RNA greater than or equal to 1,000 copies/ml
  • Documentation of maternal HIV infection by country appropriate National Guidelines
  • Signed informed consent from parent or legal guardian. An informed assent document will be provided for children 8 years of age or older when appropriate.
  • Subjects must be able to be followed at a participating clinical site
  • Subjects may be co enrolled in clinical trials for treatment of HIV infection, opportunistic infections, or other HIV related effects

Exclusion criteria

  • Children who are born to an HIV infected mother, but are uninfected or of indeterminate HIV infection status
  • Children who are orphans without legal guardians or are wards of the state

Treatment and study plan

Secondary outcomes

  1. HIV RNA copies

    Time frame: q 6 months

    characterize complications from both the disease and its treatments

  2. CD4 + T cell count

    Time frame: q 6 months

    characterize complications from both the disease and its treatments

  3. medical history

    Time frame: q 6 months

    characterize complications from both the disease and its treatments

  4. hematology and chemistry labs

    Time frame: q 6 months

    characterize complications from both the disease and its treatments

Sponsors and collaborators

Lead sponsor

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Nih

Registry information

Important dates

Study start
2002
Primary completion
2011
Study completion
2020
First posted
Jun 21, 2006
Registry last updated
Jul 30, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.