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CompletedNCT01210924CN-PARTUpdated Mar 30, 2018

Chinese Network of Pediatric Antiretroviral Therapy

An observational study in Acquired Immunodeficiency Syndrome, sponsored by National Center for AIDS/STD Control and Prevention, China CDC. Completed at 1 site in China. Open to participants aged Up to 15 Years. Per ClinicalTrials.gov, last updated 2018-03-30.

Sponsored by National Center for AIDS/STD Control and Prevention, China CDC · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
400
Ages
Up to 15 Years
Sex
All
01

Study summary

This is an observational cohort in pediatric HIV patients in China. Children who receive antiretroviral drugs will be recruited in this study. The main objectives are as follows: 1. To establish simpler and smarter pediatric antiretroviral therapy in China including both first-line and second-line regimens. 2. To study the nature, characteristics and mechanisms of immunoreconstitution in HIV-infected children using the data and samples from the pediatric antiretroviral therapy cohort. 3. To establish a basic science and clinical research network based on the pediatric antiretroviral cohort.

02

Conditions studied

  • Acquired Immunodeficiency Syndrome

Keywords

  • children
  • Acquired Immunodeficiency Syndrome
  • antiretroviral therapy
  • China
  • Mortality
03

In context

Acquired Immunodeficiency Syndrome

2,040 studies on the registry are indexed under Acquired Immunodeficiency Syndrome; 272 are open to participants now.

This study's enrollment of 400 is above the median of 236 across 355 observational studies indexed under Acquired Immunodeficiency Syndrome.

Browse Acquired Immunodeficiency Syndrome studies →

Lead sponsor

National Center for AIDS/STD Control and Prevention, China CDC is the lead sponsor of 9 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 15 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Pediatric HIV-infected patients receiving triple antiretroviral drugs

Inclusion criteria

  • clinical diagnosis of HIV infection
  • receiving triple antiretroviral drugs

Exclusion criteria

Exclusion Criteria:

  • clinical status not stable
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
400 participants (actual)
Biospecimen retention
Samples with dna

Groups and cohorts

  • Pediatric ART patients
06

What researchers measure

Primary outcomes

  1. The immunology and virologic outcomes

    Time frame: 2016

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Study locations

1 site
  • National Center for AIDS/STD Control and Prevention, China Center for Disease Control and Prevention
    Beijing, 102206, China
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 30, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01210924
Lead sponsor
National Center for AIDS/STD Control and Prevention, China CDC
Responsible party
Sponsor
First posted
Sep 29, 2010
Start date
Apr 2010
Primary completion
Dec 2015
Completion
Dec 2015
Last update
Mar 30, 2018

Study contacts

Fujie Zhang, MD
principal investigator · National Center for AIDS/STD control and prevention

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2013. You cannot join it, but the record below documents what was studied.

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