Clinic-based ART Diagnostic Evaluation

HIV Infection Clinical Trial

— CLADE  

Official title:

Clinic-based ART Diagnostic Evaluation

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01791556
• Other study ID #: WRAIR# 1591
• Secondary ID: KEMRI SSC# 1717R
• Status: Completed
• Phase: N/A
• Start date: January 26, 2010
• Est. completion date: August 2012

Study information

• Verified date: December 2023
• Source: Walter Reed Army Institute of Research (WRAIR)
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study is funded through the Office of the Global AIDS Coordinator (OGAC #KE-07-0044). The purpose of this study is two-fold. The first purpose is to see if routine monitoring of the level of HIV virus in the blood (viral load) every six months is superior to monitoring by standard clinical evaluations and or immune status (CD4 count) with intermittent viral load monitoring in adults receiving antiretroviral therapy (ART). The second purpose is to understand the cost implications and possible benefits of routine HIV viral load monitoring.

Description:

The Kenya Ministry of Health (MoH) guidelines for antiretroviral therapy (ART) and manual for ART providers recommend targeted viral load monitoring in ART management. While only limited use of viral load monitoring exist due to limitations in technical and financial resources, the feasibility and cost-effectiveness of viral load monitoring has not been prospectively studied in ART roll-out at the clinic level. "Clinic-based ART Diagnostic Evaluation" (CLADE) is an unblinded, randomized (1:1), prospective, observational, cohort public health evaluation (PHE) aimed at evaluating the superiority and cost-effectiveness of two recommended Ministry of Health ART diagnostic evaluation approaches at the clinic level in adult treatment naive patients beginning Ministry of Health approved first-line ART: "routine care", the most common approach to ART roll-out where clinical (World Health Organization) staging and immunological (CD4) monitoring are the primary baseline and follow-up evaluations and targeted viral load monitoring; and "viral load care", where routine viral loads are included with clinical and immunological evaluations. In this study we plan to enroll 820 adult participants starting ART, 410 people will be enrolled in each of the public health evaluation arms. Arm A/ "routine care" will receive MoH standard of care monitoring consisting of baseline CD4 and WHO staging every 6 months, or as clinically indicated, with CD4 and WHO staging criteria guiding care and treatment in addition to routine clinical evaluations. In addition, MoH criteria for targeted viral load monitoring will be used. Arm B/ "viral load guided care" will receive MoH standard of care as in Arm A but also have routine viral load monitoring at baseline and every 6 months, or as clinically indicated, to guide care and treatment. Each arm will receive Kenya Ministry of Health first-line ART. Participants meeting MoH criteria for treatment failure will being second-line ART.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 820
• Est. completion date: August 2012
• Est. primary completion date: March 25, 2011
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female > 18 years of age at the time of consent.
• Identified by clinic staff as intending to start ART at the next clinic visit
• Provision of informed consent in either Kiswahili, Luo or English

Exclusion Criteria:

• Any reason (medical, physical location of home relative to clinic, or other) existing that the ART team feel will prohibit the volunteer from coming for routine ART clinic visits.
• Any reason (medical, social, or other) existing that the ART team or study team feel may present a risk to the participant that outweighs the benefit of participating in the study.
• Pregnancy (confirmed or suspected) at time of enrollment.

Related Conditions & MeSH terms

• Acquired Immunodeficiency Syndrome
• Communicable Diseases
• HIV Infection
• HIV Infections
• Immunologic Deficiency Syndromes
• Infections
• RNA Virus Infections
• Virus Diseases

Intervention

Other:
• HIV-1 viral load testing

Locations

Country	Name	City	State
Kenya	Kenya Medical Research Institute/ Walter Reed Project HIV Program	Kericho

Sponsors (3)

Lead Sponsor	Collaborator
Walter Reed Army Institute of Research (WRAIR)	Kenya Medical Research Institute, US Military HIV Research Program

Country where clinical trial is conducted

Kenya, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Viral failure	The study primary endpoint is viral failure at the 18 month follow-up visit as defined by VL>1000 copies/mL by the viral load platform approved by the Kenya Medical Research Institute/ Walter Reed Project Clinical Research Center laboratory under the College of American Pathologist and related external quality assurance programs.; Relative cost-effectiveness of routine viral load monitoring in addition to CD4 count and clinical monitoring compared to CD4 and clinical alone in clinic-based ART management	18 months on follow-up
Secondary	Viral failures	Combined clinical outcome as defined by 2 new World Health Organization stage III events or 1 new World Health Organization stage IV event.; Death (as confirmed by medical records or death certificate).; Hospitalization (for any illness).; Opportunistic infections (onset after study entry).; Adherence (routinely captured by clinics).; Lost of follow-up (defined as missing 2 consecutive appointments and/or inability to have final study visit).; HIV genotype resistance in all treatment failures and all viral failures at the final study visit.; Feasibility of rolling out viral load monitoring in rural district-level ART clinics (based upon knowledge, attitudes, and performance indicators.); Cost of viral load monitoring (in addition to CD4 count and clinical care monitoring as actual costs collected during 18 months of follow-up on ART).; Adherence to GCP (as a research study is incorporated in to ART clinics and based upon GCP indicators).	18 months on follow-up