Evaluation of the Efficacy of Rasagiline in Apathy in Drug-naïve Patients With Parkinson's Disease by a Multi-center Study
Evaluation of the Efficacy of Rasagiline in Apathy in Drug-naïve Patients With Parkinson's Disease by a Multi-center, Randomized, Double-blind, Parallel-group, Placebo-controlled Study.
Among the psychiatric symptoms observed in the premotor phase of Parkinson's disease (PD) and/or in "de novo" patients, apathy is relatively frequent (estimated to 23%). However, the neuropathological bases of apathy are still unknown. However, recent data suggests that apathy could be linked to a more specific dopaminergic denervation in the ventral striatum.
Rasagiline increases the bioavailability of striatal endogenous dopamine by blocking the MAO-B. Some recent data suggest rasagiline could be effective to improve apathy in Parkinson's disease.
The primary outcome is to demonstrate a significant reduction of apathy using the Lille apathy rating scale (LARS) in drug naive patients with early diagnosed Parkinson's disease, using a treatment by rasagiline.
연구 개요
상세 설명
Study design :
Randomized, double-blind, rasagiline (1 mg) vs placebo study. Parallel group (randomization 1/1). Duration 3 months 16 recruiting centers in France
Population :
50 drug-naïve patients with Parkinson's disease, with apathy. 2 groups : 25 patients with placebo and 25 patients with rasagiline.
3 visits
- Visit 1 : inclusion / randomisation/ first study medication dispensation
- Visit 2 (1.5 month after V1) : first evaluation and second study medication dispensation.
- Visit 3 (3 months after V1, final visit) : second evaluation
연구 유형
등록 (예상)
단계
- 4단계
연락처 및 위치
연구 장소
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Clermont-Ferrand, 프랑스, 63003
- CHU clermont-ferrand
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Drug-naïve patients with Parkinson's disease (UKPDBB criteria)
- No dementia (Mattis dementia rating scale > 130; Mini Mental Sate Examination ≥26)
- No depression (MADRS < 15)
- Criteria of apathy from Robert et al (2009)
- At least mild apathy (≥-21 to Lille Apathy Rating Scale)
- Age : 35-70 y
- Affiliation to social security
- Agreement of patients
Exclusion Criteria:
- - Any antiparkinsonian treatment (L.dopa, dopamine agonists, MAO-B-I, amantadine, anticholinergics). Patients treated by dopamine agonists but who have stopped it more than 3 months before their inclusion can be included.
- Ongoing severe psychiatric or somatic diseases
- Others treatments :
- antipsychotics
- antidepressants and anxiolytics (exclusion if the treatment is not stable the month before inclusion)
- psychostimulants (methylphenidate, adrafinil, modafinil, deanol, vitamin C, sulbutiamine, glutamic acid, aspartic acid)
- any contra-indication according to SmPC
- patients under guardianship
- Women without efficient contraception
- Person who participate to an other study
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 더블
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: rasagiline
Randomized, double-blind, rasagiline (1 mg) vs placebo study.
Parallel group (randomization 1/1).
Duration 3 months 16 recruiting centers in France
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|
|
위약 비교기: placebo
Randomized, double-blind, rasagiline (1 mg) vs placebo study.
Parallel group (randomization 1/1).
Duration 3 months 16 recruiting centers in France
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
|
Lille Apathy Rating Scale (LARS) score
기간: at the visit 3 (after 3 months of treatment)
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at the visit 3 (after 3 months of treatment)
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2차 결과 측정
결과 측정 |
기간 |
|---|---|
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Motor assessment : Unified Parkinson's Disease Rating Scale
기간: at the visit 3 (after 3 months of treatment)
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at the visit 3 (after 3 months of treatment)
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Depressive and anxiety symptoms : MADRS + Hamilton anxiety scale
기간: at the visit 3 (after 3 months of treatment)
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at the visit 3 (after 3 months of treatment)
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Self assessment of apathy : Starkstein
기간: at the visit 3 (after 3 months of treatment)
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at the visit 3 (after 3 months of treatment)
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Quality of life : PDQ 39
기간: at the visit 3 (after 3 months of treatment)
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at the visit 3 (after 3 months of treatment)
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Cognitive assessment: MATTIS dementia rating scale, MMSE, executive functions battery
기간: at the visit 3 (after 3 months of treatment)
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at the visit 3 (after 3 months of treatment)
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Hyperdopaminergic symptoms : Parkinson's disease behavioral scale
기간: at the visit 3 (after 3 months of treatment)
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at the visit 3 (after 3 months of treatment)
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Fatigue assessment : Parkinson Fatigue Scale
기간: at the visit 3 (after 3 months of treatment)
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at the visit 3 (after 3 months of treatment)
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공동 작업자 및 조사자
협력자
수사관
- 수석 연구원: Denis PEZET, University Hospital, Clermont-Ferrand
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (예상)
연구 완료 (예상)
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
추가 관련 MeSH 약관
기타 연구 ID 번호
- CHU-0138
- 2007-002800-16
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