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

20. november 2014 opdateret af: Christine A. Wanke, Tufts University

Economic Evaluation of Treatment of HIV With Zidovudine/Stavudine and Tenofovir Regimen: A Cost Effectiveness Study

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.

Studieoversigt

Status

Afsluttet

Betingelser

Detaljeret beskrivelse

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.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

68

Fase

  • Fase 4

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • Tamilnadu
      • Vellore, Tamilnadu, Indien, 632004
        • Christian Medical College

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

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

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv komparator: Zidovudine
zidovudine 300 mg + lamivudine 150 mg + nevirapine 200 mg , once daily, for a year
zidovudine 300 mg + lamivudine 150 mg + nevirapine 200 mg , once daily, for a year
Andre navne:
  • Lazid-N
  • Duovir-N
  • Zidolam-N
Aktiv komparator: Tenofovir
tenofovir 300 mg+ emtricitabine 200 mg + efavirenz 600 mg, once daily, for one year
tenofovir 300 mg+ emtricitabine 200 mg + efavirenz 600 mg, once daily, for one year
Andre navne:
  • Atripla
  • Vonavir

Hvad måler undersøgelsen?

Primære resultatmål

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

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Studiestol: Christine C Wanke, MD, Tufts University
  • Ledende efterforsker: Sowmyanarayanan V Thuppal, MD, Tufts University

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. november 2012

Primær færdiggørelse (Faktiske)

1. august 2014

Studieafslutning (Faktiske)

1. august 2014

Datoer for studieregistrering

Først indsendt

18. september 2012

Først indsendt, der opfyldte QC-kriterier

25. september 2012

Først opslået (Skøn)

26. september 2012

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

24. november 2014

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

20. november 2014

Sidst verificeret

1. november 2014

Mere information

Begreber relateret til denne undersøgelse

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med HIV

Kliniske forsøg med Zidovudine

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