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Pediatric Urgent Start of Highly Active Antiretroviral Treatment (HAART) (PUSH)

Primary Purpose

Human Immunodeficiency Virus, Immune Reconstitution Inflammatory Syndrome

Status
Completed
Phase
Not Applicable
Locations
Kenya
Study Type
Interventional
Intervention
Urgent ART
Early ART
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Human Immunodeficiency Virus focused on measuring HIV-1, IRIS

Eligibility Criteria

undefined - 12 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Aged ≤ 12 years old (reported)
  • HIV-1 positive (for example, two rapid HIV-1 antibody tests for children >18 months and not breastfeeding, or one HIV-1 DNA/RNA test for children ≤18 months or who are breastfeeding)
  • Not currently receiving antiretroviral therapy (history of pMTCT does not affect eligibility)
  • Eligible to receive ART, according to current WHO guidelines
  • Caregiver plans to reside in study catchment area for at least 6 months (reported)
  • Caregiver provides sufficient locator information

Exclusion Criteria:

  • Suspected meningitis, any other central nervous system infection, or encephalitis

Sites / Locations

  • JOOTRH
  • Kisumu District Hospital
  • Mbagathi District Hospital
  • Kenyatta National Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Urgent ART

Early ART

Arm Description

Initiation of highly active antiretroviral therapy (HAART) within 48 hours of enrollment. Antiretroviral therapy will include regimens recommended by the Kenyan Ministry of Health.

Initiation of HAART 7-14 days after enrollment.

Outcomes

Primary Outcome Measures

All-cause Mortality

Secondary Outcome Measures

Number of Participants With Evidence of Immune Reconstitution and Inflammatory Syndrome (IRIS)
Confirmed, possible or likely IRIS based on external independent review
Number of Participants With Potential Drug Toxicity
Participants with adverse events that are deemed to be potentially related to medications.

Full Information

First Posted
August 21, 2012
Last Updated
April 11, 2018
Sponsor
University of Washington
Collaborators
University of Nairobi, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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1. Study Identification

Unique Protocol Identification Number
NCT02063880
Brief Title
Pediatric Urgent Start of Highly Active Antiretroviral Treatment (HAART)
Acronym
PUSH
Official Title
Urgent Versus Post-Stabilization ART in HIV-1 Infected Children With Severe Co-Infections
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
March 2013 (undefined)
Primary Completion Date
November 2015 (Actual)
Study Completion Date
November 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
University of Nairobi, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Design: Randomized clinical trial involving hospitalized HIV-1 infected children. Children will be randomized to randomized to urgent (<48 hours) versus early antiretroviral therapy (7-14 days). This trial will be unblinded. Population: Hospitalized HIV-1 infected children who are antiretroviral therapy (ART) naïve ≤ 12 years of age. Sample size: 360 children will be randomized (180 per arm). Treatment: All infants will be treated with ART according to World Health Organization (WHO) and Kenyan national guidelines. Study duration: Enrollment into the study will occur over the course of 36-48 months and each infant will be routinely followed for a maximum of 6 months. Study site: Kenyan hospitals. Primary hypothesis: HIV-1 infected children hospitalized with severe co-infection either may be unsalvageable due to too far advanced immunosuppression/co-infection or may benefit from urgent ART. Secondary hypotheses: Urgent ART during an acute infection could potentially result in increased risk of immune reconstitution inflammatory syndrome (IRIS) or drug toxicities/interactions. Specific aims: To compare the 6 month all-cause mortality rate, incidence of immune reconstitution inflammatory syndrome (IRIS), and incidence of drug toxicity in HIV-1 infected children (≤ 12 years old) presenting to hospital with a serious infection randomized to urgent (<48 hours) versus early ART (7-14 days). To determine co-factors for mortality, IRIS, and drug toxicity. Potential cofactors will include: baseline weight-for-age, height-for-age, weight-for-height (Z-scores), CD4, HIV-1 RNA, type of co-infection, age, rate of viral load and CD4 change following ART, immune activation markers, pathogen and HIV-1 specific immune responses. Secondary aim: To determine etiologies of IRIS and to compare immune reconstitution to HIV, TB, EBV and CMV following ART overall and in each trial arm.
Detailed Description
Children will be followed and compared for 6-month mortality.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Human Immunodeficiency Virus, Immune Reconstitution Inflammatory Syndrome
Keywords
HIV-1, IRIS

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
183 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Urgent ART
Arm Type
Experimental
Arm Description
Initiation of highly active antiretroviral therapy (HAART) within 48 hours of enrollment. Antiretroviral therapy will include regimens recommended by the Kenyan Ministry of Health.
Arm Title
Early ART
Arm Type
Active Comparator
Arm Description
Initiation of HAART 7-14 days after enrollment.
Intervention Type
Other
Intervention Name(s)
Urgent ART
Other Intervention Name(s)
HAART regimens recommended by WHO and Kenya MOH.
Intervention Description
Children will be started on HAART <48 hours after enrollment.
Intervention Type
Other
Intervention Name(s)
Early ART
Intervention Description
Children will be started on ART after stabilization 7-14 days after enrollment.
Primary Outcome Measure Information:
Title
All-cause Mortality
Time Frame
6 months post-HAART initiation
Secondary Outcome Measure Information:
Title
Number of Participants With Evidence of Immune Reconstitution and Inflammatory Syndrome (IRIS)
Description
Confirmed, possible or likely IRIS based on external independent review
Time Frame
6 months post-HAART initiation
Title
Number of Participants With Potential Drug Toxicity
Description
Participants with adverse events that are deemed to be potentially related to medications.
Time Frame
6 months post-HAART initiation

10. Eligibility

Sex
All
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged ≤ 12 years old (reported) HIV-1 positive (for example, two rapid HIV-1 antibody tests for children >18 months and not breastfeeding, or one HIV-1 DNA/RNA test for children ≤18 months or who are breastfeeding) Not currently receiving antiretroviral therapy (history of pMTCT does not affect eligibility) Eligible to receive ART, according to current WHO guidelines Caregiver plans to reside in study catchment area for at least 6 months (reported) Caregiver provides sufficient locator information Exclusion Criteria: Suspected meningitis, any other central nervous system infection, or encephalitis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Grace John Stewart, MD, PhD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
JOOTRH
City
Kisumu
Country
Kenya
Facility Name
Kisumu District Hospital
City
Kisumu
Country
Kenya
Facility Name
Mbagathi District Hospital
City
Nairobi
ZIP/Postal Code
0202
Country
Kenya
Facility Name
Kenyatta National Hospital
City
Nairobi
Country
Kenya

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
after primary and secondary outcomes are published
Citations:
PubMed Identifier
31095004
Citation
Njuguna IN, Cranmer LM, Wagner AD, LaCourse SM, Mugo C, Benki-Nugent S, Richardson BA, Stern J, Maleche-Obimbo E, Wamalwa DC, John-Stewart G. Brief Report: Cofactors of Mortality Among Hospitalized HIV-Infected Children Initiating Antiretroviral Therapy in Kenya. J Acquir Immune Defic Syndr. 2019 Jun 1;81(2):138-144. doi: 10.1097/QAI.0000000000002012.
Results Reference
derived
PubMed Identifier
29324985
Citation
LaCourse SM, Cranmer LM, Njuguna IN, Gatimu J, Stern J, Maleche-Obimbo E, Walson JL, Wamalwa D, John-Stewart GC, Pavlinac PB. Urine Tuberculosis Lipoarabinomannan Predicts Mortality in Hospitalized Human Immunodeficiency Virus-Infected Children. Clin Infect Dis. 2018 May 17;66(11):1798-1801. doi: 10.1093/cid/ciy011.
Results Reference
derived
PubMed Identifier
29150377
Citation
Njuguna IN, Cranmer LM, Otieno VO, Mugo C, Okinyi HM, Benki-Nugent S, Richardson B, Stern J, Maleche-Obimbo E, Wamalwa DC, John-Stewart GC. Urgent versus post-stabilisation antiretroviral treatment in hospitalised HIV-infected children in Kenya (PUSH): a randomised controlled trial. Lancet HIV. 2018 Jan;5(1):e12-e22. doi: 10.1016/S2352-3018(17)30167-4. Epub 2017 Nov 14.
Results Reference
derived
PubMed Identifier
28609404
Citation
Wagner AD, Njuguna IN, Andere RA, Cranmer LM, Okinyi HM, Benki-Nugent S, Chohan BH, Maleche-Obimbo E, Wamalwa DC, John-Stewart GC. Infant/child rapid serology tests fail to reliably assess HIV exposure among sick hospitalized infants. AIDS. 2017 Jul 17;31(11):F1-F7. doi: 10.1097/QAD.0000000000001562.
Results Reference
derived
PubMed Identifier
27308805
Citation
Njuguna IN, Wagner AD, Cranmer LM, Otieno VO, Onyango JA, Chebet DJ, Okinyi HM, Benki-Nugent S, Maleche-Obimbo E, Slyker JA, John-Stewart GC, Wamalwa DC. Hospitalized Children Reveal Health Systems Gaps in the Mother-Child HIV Care Cascade in Kenya. AIDS Patient Care STDS. 2016 Mar;30(3):119-24. doi: 10.1089/apc.2015.0239.
Results Reference
derived

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Pediatric Urgent Start of Highly Active Antiretroviral Treatment (HAART)

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