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Completed

NCT Number: NCT03120065

Virologic Treatment Failure and Drug Resistance in HIV-infected Kenyan Children (RESPECT)

The primary objective of this study is to use a well-characterized pediatric AMPATH cohort, with detailed medication-taking, drug level, and clinical data, to longitudinally evaluate treatment failure and drug resistance to improve long-term care for HIV-infected children in Kenya and other RLS. Examining treatment failure and drug resistance emergence in children on ART and what factors impact these negative outcomes, will provide needed data to critically evaluate the efficacy of current ART, weight-based pediatric drug dosing guidelines, and recommendations for subsequent therapies. The objective is to specifically characterize how non-adherence leads to a lack of viral suppression and to drug resistance evolution, and how this characterization can inform interventions to improve adherence and increase treatment success.

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Key information

Age range

4 year–19 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Moi Teaching and Referral Hospital - AMPATH Center

Eldoret, 30100, Kenya

About this study

Resistance to antiretroviral therapy (ART) hampers effective treatment of pediatric HIV infection and can undermine long-term clinical care outcomes. In resource-limited settings (RLS), where 90% of the world's HIV-infected children live, the risk and impact of ART failure and resistance development are particularly significant due to limited treatment monitoring, restricted medication options and lifelong ART needs, from birth through adolescence and into adulthood. Children in RLS therefore face serious clinical consequences when their virus is not suppressed, but few longitudinal data are available to inform pediatric clinical guidelines or direct interventions to minimize those risks. How specific patterns of medication non-adherence or challenges with appropriate ART dosing might impact ART failure and the development of drug resistance are poorly understood for children in RLS. The primary objective of this study is to use a well-characterized pediatric AMPATH cohort, with detailed medication-taking, drug level, and clinical data, to longitudinally evaluate treatment failure and drug resistance to improve long-term care for HIV-infected children in Kenya and other RLS. Examining treatment failure and drug resistance emergence in children on ART and what factors impact these negative outcomes, will provide needed data to critically evaluate the efficacy of current ART, weight-based pediatric drug dosing guidelines, and recommendations for subsequent therapies. The objective is to specifically characterize how non-adherence leads to a lack of viral suppression and to drug resistance evolution, and how this characterization can inform interventions to improve adherence and increase treatment success. AMPATH cares for over 80,000 adult and pediatric HIV-infected patients in western Kenya, including over 2,800 children on ART.

The research objective of this application will be accomplished by pursuing the following five specific aims: Aim 1: Determine prevalence of viral failure and examine resistance mutations among a retrospective study cohort of 685 perinatally HIV-infected Kenyan children on 1st-line ART; Aim 2: Investigate associations between specific adherence patterns, ART drug levels and other demographic and clinical factors, with viral failure and drug resistance; Aim 3: Study long-term immunologic, virologic and drug resistance outcomes and their associations in prospectively re-enrolled study participants; Aim 4: Enhance analyses of viral failure, drug resistance accumulation and associated demographic and clinical factors by examining the longitudinal banked samples available for a subset of the study cohort (n=327); Aim 5: Develop a data-driven intervention algorithm to identify children at risk for viral failure and resistance.

The hypothesis of this study proposes that there will be high levels of treatment failure and drug resistance associated with patterns of non-adherence and inadequate drug levels.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Previous enrollment in CAMP study
  • Viable banked blood sample; HIV-infected documented by DNA-PCR (Amplicor, Roche, Basel, Switzerland) for children less than 18 months of age and by 2 parallel HIV rapid ELISA tests using Determine and Bioline for children older than 18 months of age.
  • < 19 years of age

Exclusion criteria

Mental or physical incapacity of legal caregiver leading to inability to provide informed consent

Treatment and study plan

Electronic Dose Monitoring (MEMS)

Other

The MEMS cap is an electronic bottle cap that records the time and date of a bottle being opened. The research personnel will extract the timing of the MEMS bottle opening events for adherence analysis.

Primary outcomes

  1. Viral Resistance

    Time frame: 18 months

    Blood samples will be analyzed for viral resistance testing, both for retrospective and prospective samples samples (TP1)

Secondary outcomes

  1. Adherence MEMS

    Time frame: 3 months

    Adherence will be monitored via MEMS bottle caps

  2. Adherence CAMP

    Time frame: 3 months

    Adherence will be assessed via CAMP questionnaire

  3. Clinical Data: WHO stage

    Time frame: 6 years

    WHO stage will be analyzed for associations with viral resistance and treatment failure in this cohort.

  4. Clinical Data: Viral Load

    Time frame: 6 years

    Longitudinal viral loads will be analyzed for associations with viral resistance and treatment failure in this cohort.

  5. Clinical Data: Weight

    Time frame: 6 years

    Longitudinal weight will be analyzed for associations with viral resistance and treatment failure in this cohort.

  6. Clinical Data: Height

    Time frame: 6 years

    Longitudinal height will be analyzed for associations with viral resistance and treatment failure in this cohort.

  7. Clinical Data: Regimen

    Time frame: 6 years

    Longitudinal regimen will be analyzed for associations with viral resistance and treatment failure in this cohort.

  8. Clinical Data: Opportunistic Infections

    Time frame: 6 years

    Longitudinal opportunistic infections will be analyzed for associations with viral resistance and treatment failure in this cohort.

  9. Clinical Data: Disclosure Status

    Time frame: 6 years

    Longitudinal disclosure status will be analyzed for associations with viral resistance and treatment failure in this cohort.

Sponsors and collaborators

Lead sponsor

Rachel Vreeman, MD, MS

Other

Collaborators

  • Brown University
  • Moi University

Registry information

Official study title

Virologic Treatment Failure and Drug Resistance in HIV-infected Kenyan Children

Acronym: RESPECT

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Apr 19, 2017
Registry last updated
Jul 22, 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.

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