Economic, Clinical and Quality of Life Assessment in Patients on Antiretroviral Therapy

Phase 4

Completed

• Conditions: HIV
• Interventions: Drug: Tenofovir; Drug: Zidovudine

• Registration Number: NCT01694017
• Lead Sponsor: Tufts University

Brief Summary

The purpose of this study is to compare clinical, economical and quality of life (QOL) outcomes in patients living with HIV on zidovudine/stavudine regimen and tenofovir regimen. This study will be an unblinded randomized trial. The first step will be empirical data collection for one year for calculating the incremental cost effectiveness ratio (ICER). The second step will be to perform a simulation model for calculating long term ICER.

Detailed Description

The drug regimen for treatment of HIV at the free ART centers in India includes stavudine/zidovudine and lamivudine with nevirapine. Approximately 20-30% of the patients on this regimen experience drug toxicity within the first six months of treatment.

The tenofovir based regimen is one of the least toxic regimens with less than 5% of patients experiencing toxicity. Tenofovir based regimen is not considered as the first choice for ART in the Indian governmental program, because it is more expensive than the other drug regimens, in spite of better clinical outcomes in resource limited settings. The cost of treatment with stavudine/zidovudine is presumed to be less expensive and is the preferred first line treatment, but we believe that although the direct cost to the government is less, patients on zidovudine/stavudine regimen have to spend more money for additional hospital visits and admissions, laboratory investigations and other medications due to ART induced toxicity.

There are no published data including economic, clinical and quality of life outcomes to compare the two regimens from India. Hence, this unblinded randomized pragmatic comparative effectiveness study will seek to identify the best treatment for HIV patients based on the incremental cost effectiveness ratio (ICER), quality of life (QOL) and clinical outcomes.

The clinical outcomes include viral suppression, change in the CD4 and proportion of patients with toxicity and opportunistic infections. Direct costs for the treatment will be calculated. The QOL scores will be estimated and compared between the regimens using questionnaires. QOL scores and direct cost will be used as utilities for calculating ICER.

Study Timeline

• Study First Submitted: 2012-09-18
• Study First Submitted QC: 2012-09-25
• Study First Posted: 2012-09-26
• Study Start: 2012-11
• Primary Completion: 2014-08
• Study Completion: 2014-08
• Status Verified: 2014-11
• Last Update Submitted: 2014-11-20
• Last Update Posted: 2014-11-24

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 68

Inclusion Criteria

• All treatment naïve patients above 18 years confirmed with the diagnosis of HIV
• Eligible for initiation of cART based on the National Aids Control Organization of India
• Consenting for participation and follow-up for one year.

Exclusion Criteria

• All patients requiring hospitalization at the time of initiation of treatment
• Patients with opportunistic infections including tuberculosis
• Patients with co-morbidities like diabetes or neurological impairments
• Pregnant and breast feeding women and children less than 18 years will be excluded
• All patients living outside the catchment area of CMC and not willing for regular follow-up will be excluded
• Patients with a creatinine clearance less than 50 mL/min will be excluded.
• Patients receiving other co-medications with possible interaction with tenofovir, like antifungal (voriconazole), ergot derivatives (dihydroergotamine, ergonovine, ergotamine, and methylergonovine), benzodiazepines (midazolam, triazolam), calcium channel blocker (bepridil), GI motility agent (cisapride), neuroleptic (pimozide) and St.John's wort will be excluded.
• Patients with hemoglobin less than 8 gm/dl
• Patients started on tenofovir regimen by the treating physician at the time of enrollment will be excluded

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Tenofovir	Tenofovir	tenofovir 300 mg+ emtricitabine 200 mg + efavirenz 600 mg, once daily, for one year
Zidovudine	Zidovudine	zidovudine 300 mg + lamivudine 150 mg + nevirapine 200 mg , once daily, for a year

Primary Outcome Measures

Name	Time	Method
Quality of life	Month 1 and end of months 4,8 and 12
Change in CD4 levels	End of Months 6 and 12
Direct costs	Months: 1,2,3,4,5,6,7,8,9,10,11,12
Viral suppression	End of follow-up : end of 12th Month
Drug related toxicity	Months : 1,2,3,4,5,6,7,8,9,10,11,12
opportunistic infections	Months: 1,2,3,4,5,6,7,8,9,10,11,12

Trial Locations

Locations (1)

Christian Medical College; 🇮🇳 Vellore, Tamilnadu, India