HIV Viral Load Monitoring in Resource-Poor Settings - Full Text View

Sponsor:	University of Alabama at Birmingham
Collaborator:	Adult AIDS Clinical Trials Group
Information provided by (Responsible Party):	Michael Saag, MD, University of Alabama at Birmingham
ClinicalTrials.gov Identifier:	NCT00929604

Purpose

No randomized clinical trial to date has demonstrated a survival benefit of using regular HIV-1 ribonucleic acid (RNA) viral load (VL) testing to monitor patients' responses to antiretroviral therapy (ART) for HIV infection. The measurement of VL is recommended to monitor the response to ART in developed countries. In resource-constrained settings, the World Health Organization (WHO) does not recommend routine VL testing, in part due to the cost and complex infrastructure needed for reliable results. In these settings, WHO has proposed the use of clinical and CD4+ lymphocyte-based criteria to guide treatment decisions. However, multiple studies have demonstrated the poor performance of these criteria in sub-Saharan Africa and the frequent discordance between immunologic and virologic responses to ART.

The use of routine viral load monitoring should be evaluated in resource-constrained settings. The investigators hypothesize that routine viral load testing of patients on ART will improve patient survival, decrease disease progression and development of drug resistance, and will be feasible and cost-effective for resource-constrained settings.

Condition	Intervention
HIV AIDS HIV Infections	Other: HIV-1 viral load testing

Study Type:	Interventional
Study Design:	Allocation: Randomized Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Health Services Research
Official Title:	Effectiveness of HIV Viral Load Monitoring of Patient Outcome in Resource-Poor Settings

Resource links provided by NLM:

Genetics Home Reference related topics: complement factor I deficiency

MedlinePlus related topics: HIV/AIDS

U.S. FDA Resources

Further study details as provided by University of Alabama at Birmingham:

Primary Outcome Measures:

Patient survival [ Time Frame: 36 months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:

To assess HIV clinical disease progression (weight, CD4 cell response, incident opportunistic infections) [ Time Frame: 36 months ] [ Designated as safety issue: No ]
To assess the impact of more rapid ART regimen switching on available second and third-line treatment options [ Time Frame: 36 months ] [ Designated as safety issue: No ]
To monitor the effectiveness of newer antiretroviral medications introduced in Zambia (principally tenofovir) [ Time Frame: 36 months ] [ Designated as safety issue: No ]
To characterize the timing and sequence of HIV drug resistance development among patients in each study arm [ Time Frame: 36 months ] [ Designated as safety issue: No ]
To assess the feasibility, acceptability, and cost effectiveness of the two management strategies in a resource-constrained sub-Saharan African setting [ Time Frame: 36 months ] [ Designated as safety issue: No ]

Enrollment:	2112
Study Start Date:	December 2006
Estimated Study Completion Date:	October 2012
Primary Completion Date:	May 2011 (Final data collection date for primary outcome measure)

Arms	Assigned Interventions
No Intervention: Standard of care Standard of care arm: utilizes the current standard of care per Zambian national guidelines to determine treatment failure and eligibility for second-line ART. HIV-1 viral load measurement is performed if the criteria for either immunologic (i.e., CD4+ lymphocyte count-based) or clinical treatment failure are fulfilled. If both immunologic and clinical treatment failure criteria are fulfilled, the ART regimen is changed to second-line without VL testing.
Experimental: Routine HIV-1 viral load testing Routine viral load testing arm: Routine HIV viral load testing at ART initiation (baseline) and at 3, 6, 12, 18, 24, 30 and 36 months thereafter.	Other: HIV-1 viral load testing Plasma HIV-1 RNA viral load testing performed at ART initiation (baseline) and at 3, 6, 12, 18, 24, 30, and 36 months thereafter. Routine viral load results are provided to clinicians for the management of the participant's HIV treatment. Other Name: Viral load measured by the Roche Amplicor HIV-1 RNA Monitor kit (version 1.5; Roche Molecular Diagnostics, Pleasanton, CA, USA).

Arms

Assigned Interventions

No Intervention: Standard of care

Standard of care arm: utilizes the current standard of care per Zambian national guidelines to determine treatment failure and eligibility for second-line ART. HIV-1 viral load measurement is performed if the criteria for either immunologic (i.e., CD4+ lymphocyte count-based) or clinical treatment failure are fulfilled. If both immunologic and clinical treatment failure criteria are fulfilled, the ART regimen is changed to second-line without VL testing.

Experimental: Routine HIV-1 viral load testing

Routine viral load testing arm: Routine HIV viral load testing at ART initiation (baseline) and at 3, 6, 12, 18, 24, 30 and 36 months thereafter.

Other: HIV-1 viral load testing

Plasma HIV-1 RNA viral load testing performed at ART initiation (baseline) and at 3, 6, 12, 18, 24, 30, and 36 months thereafter. Routine viral load results are provided to clinicians for the management of the participant's HIV treatment.

Other Name: Viral load measured by the Roche Amplicor HIV-1 RNA Monitor kit (version 1.5; Roche Molecular Diagnostics, Pleasanton, CA, USA).

Detailed Description:

The study 'Effectiveness of HIV Viral Load Monitoring on Patient Outcome in Resource-Poor Settings,' is a dual-arm, cluster randomized trial to evaluate the use of routine plasma HIV-1 VL monitoring to improve survival and decrease HIV disease progression in patients receiving ART. The primary objective is to assess mortality at 36 months among ART naïve patients initiating therapy and receiving care at facilities with access to routine HIV VL testing (at ART initiation, at 3 months and at every 6 months thereafter) compared to those initiating first regimens and receiving care at facilities according to our local standard of care (which uses immunological [i.e. CD4+ lymphocyte count-based]and clinical criteria to diagnose treatment failure, with discretionary VL testing when the two do not agree).

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Documented HIV-1 infection (according to local standard rapid testing algorithms)
Age 18 years or greater
Able and willing to provide informed consent to participate
Eligible for antiretroviral therapy per Zambian national guidelines, which are any of the following:
- CD4+ cell count less than 200 cells/mm3;
- WHO Stage IV disease; or
- WHO Stage III disease and CD4+ cell count less than 350 cells/mm3
Residence in the geographical catchment area of the VLS clinic and intent to remain there for the duration of the study
Willingness to adhere to the study visit schedule and to be followed-up at home in the event of a missed study visit
Initiating ART on the day of VLS enrollment, informed consent, and baseline blood collection

Exclusion Criteria:

Receipt of more than 7 days (cumulative) of prior antiretroviral therapy at any time prior to study entry, with the exception of zidovudine and/or single dose nevirapine for prevention of mother-to-child transmission;
Any exposure to antiretroviral therapy in the past one month
A condition that, in the opinion of the investigators, would interfere with adherence to study requirements (e.g., mental illness or active drug or alcohol use or dependence)
Serious illness requiring referral to hospital at the time of ART initiation
For patients seeking care at sites randomized to the standard of care arm: participation in another research protocol that offers routine viral load testing
Unwillingness to consent to all aspects of study protocol including blood specimen storage

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00929604

Locations

Zambia
Centre for Infectious Disease Research in Zambia
Lusaka, Zambia

Sponsors and Collaborators

University of Alabama at Birmingham

Adult AIDS Clinical Trials Group

Investigators

Principal Investigator:

Michael S. Saag, M.D.

University of Alabama at Birmingham

More Information

No publications provided by University of Alabama at Birmingham

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Koethe JR, Westfall AO, Luhanga DK, Clark GM, Goldman JD, Mulenga PL, Cantrell RA, Chi BH, Zulu I, Saag MS, Stringer JS. A cluster randomized trial of routine HIV-1 viral load monitoring in Zambia: study design, implementation, and baseline cohort characteristics. PLoS One. 2010 Mar 12;5(3):e9680.

Responsible Party:	Michael Saag, MD, Director, Center for AIDS Research, University of Alabama at Birmingham
ClinicalTrials.gov Identifier:	NCT00929604 History of Changes
Other Study ID Numbers:	VLS
Study First Received:	June 25, 2009
Last Updated:	November 1, 2011
Health Authority:	Zambia: Research Ethics Committee

Keywords provided by University of Alabama at Birmingham:

HIV
AIDS
Zambia
viral load
antiretroviral therapy

cluster randomization
ART monitoring
treatment failure
randomized clinical trial
treatment naive

Additional relevant MeSH terms:

HIV Infections
Acquired Immunodeficiency Syndrome
Lentivirus Infections
Retroviridae Infections
RNA Virus Infections
Virus Diseases

Sexually Transmitted Diseases, Viral
Sexually Transmitted Diseases
Immunologic Deficiency Syndromes
Immune System Diseases
Slow Virus Diseases

ClinicalTrials.gov processed this record on May 23, 2012