- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT01694017
Economic, Clinical and Quality of Life Assessment in Patients on Antiretroviral Therapy
Economic Evaluation of Treatment of HIV With Zidovudine/Stavudine and Tenofovir Regimen: A Cost Effectiveness Study
연구 개요
상세 설명
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.
연구 유형
등록 (실제)
단계
- 4단계
연락처 및 위치
연구 장소
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Tamilnadu
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Vellore, Tamilnadu, 인도, 632004
- Christian Medical College
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
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
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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활성 비교기: Zidovudine
zidovudine 300 mg + lamivudine 150 mg + nevirapine 200 mg , once daily, for a year
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zidovudine 300 mg + lamivudine 150 mg + nevirapine 200 mg , once daily, for a year
다른 이름들:
|
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활성 비교기: Tenofovir
tenofovir 300 mg+ emtricitabine 200 mg + efavirenz 600 mg, once daily, for one year
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tenofovir 300 mg+ emtricitabine 200 mg + efavirenz 600 mg, once daily, for one year
다른 이름들:
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
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Viral suppression
기간: End of follow-up : end of 12th Month
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End of follow-up : end of 12th Month
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Change in CD4 levels
기간: End of Months 6 and 12
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End of Months 6 and 12
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Drug related toxicity
기간: Months : 1,2,3,4,5,6,7,8,9,10,11,12
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Months : 1,2,3,4,5,6,7,8,9,10,11,12
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opportunistic infections
기간: Months: 1,2,3,4,5,6,7,8,9,10,11,12
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Months: 1,2,3,4,5,6,7,8,9,10,11,12
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Direct costs
기간: Months: 1,2,3,4,5,6,7,8,9,10,11,12
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Months: 1,2,3,4,5,6,7,8,9,10,11,12
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Quality of life
기간: Month 1 and end of months 4,8 and 12
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Month 1 and end of months 4,8 and 12
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공동 작업자 및 조사자
스폰서
수사관
- 연구 의자: Christine C Wanke, MD, Tufts University
- 수석 연구원: Sowmyanarayanan V Thuppal, MD, Tufts University
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (추정)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
- 10465 (기타 식별자: Fred Hutch/University of Washington Cancer Consortium)
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
에이즈에 대한 임상 시험
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Duke UniversityGilead Sciences모병HIV 예방 | HIV 사전 노출 예방 | HIV 예방 프로그램 | HIV 예방 및 관리 | HIV 사전 노출 예방 사용미국
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Institute of HIV Research and Innovation Foundation...National Institutes of Health (NIH)모병
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Johns Hopkins UniversityNational Institute of Mental Health (NIMH)모병
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Massachusetts General HospitalNational Institute of Mental Health (NIMH)모병실행할 수 있음 | HIV 예방 | PrEP 흡수 | 수용 가능성 | HIV 자가 테스트 | HIV 음성 산후 여성의 남성 파트너남아프리카
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State University of New York at BuffaloYale University Center for Interdisciplinary Research on AIDS아직 모집하지 않음HIV 예방 | HIV 테스트 | 성 및 생식 건강미국
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Hospital Clinic of Barcelona완전한
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Thomas Aagaard RasmussenAarhus University Hospital; The Alfred; Germans Trias i Pujol Hospital; Walter and Eliza Hall...모병
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University of Minnesota빼는HIV 감염 | HIV/에이즈 | 에이즈 | 보조기구 | 에이즈/HIV 문제 | 에이즈와 감염미국
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Instituto Mexicano del Seguro Social모병체중 감량 | 에이즈 | HIV-1 감염 | 체중 변화 | HIV 관련 체중 감소 | 인테그라제 억제제, HIV; HIV 프로테아제 억제멕시코
Zidovudine에 대한 임상 시험
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University of Colorado, DenverNational Institute of Allergy and Infectious Diseases (NIAID); University of Hawaii완전한
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Assistance Publique - Hôpitaux de ParisUnité de Recherche Clinique Necker Cochin, France완전한
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ANRS, Emerging Infectious DiseasesAbbott완전한
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Centers for Disease Control and Prevention완전한
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Obafemi Awolowo UniversityLondon School of Hygiene and Tropical Medicine; University of California, San Diego; University... 그리고 다른 협력자들완전한
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Harvard School of Public Health (HSPH)National Institute of Allergy and Infectious Diseases (NIAID)종료됨