Enhancement of STroke REhabilitation with Levodopa (ESTREL): Rationale and design of a randomized placebo-controlled, double blind superiority trial.

IF 5.8 3区 医学 Q1 CLINICAL NEUROLOGY European Stroke Journal Pub Date : 2024-06-09 DOI:10.1177/23969873241255867
Annaelle Zietz, Josefin E Kaufmann, Karin Wiesner, Sandro Kevin Fischer, Martina Wiegert, Wilma Dj Verhagen-Kamerbeek, Yannik Rottenberger, Anne Schwarz, Nils Peters, Henrik Gensicke, Friedrich Medlin, Jens Carsten Möller, Bartosz Bujan, Leo H Bonati, Marcel Arnold, Sabine Schaedelin, René M Müri, Lars G Hemkens, Patrik Michel, Philippe A Lyrer, Jeremia P Held, Gary A Ford, Andreas R Luft, Christopher Traenka, Stefan T Engelter
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Abstract

Rationale: Novel therapeutic approaches are needed in stroke recovery. Whether pharmacological therapies are beneficial for enhancing stroke recovery is unclear. Dopamine is a neurotransmitter involved in motor learning, reward, and brain plasticity. Its prodrug levodopa is a promising agent for stroke recovery.

Aim and hypothesis: To investigate the hypothesis that levodopa, in addition to standardized rehabilitation therapy based on active task training, results in an enhancement of functional recovery in acute ischemic or hemorrhagic stroke patients compared to placebo.

Design: ESTREL (Enhancement of Stroke REhabilitation with Levodopa) is a randomized (ratio 1:1), multicenter, placebo-controlled, double-blind, parallel-group superiority trial.

Participants: 610 participants (according to sample size calculation) with a clinically meaningful hemiparesis will be enrolled ⩽7 days after stroke onset. Key eligibility criteria include (i) in-hospital-rehabilitation required, (ii) capability to participate in rehabilitation, (iii) previous independence in daily living.

Intervention: Levodopa 100 mg/carbidopa 25 mg three times daily, administered for 5 weeks in addition to standardized rehabilitation. The study intervention will be initiated within 7 days after stroke onset.

Comparison: Matching placebo plus standardized rehabilitation.

Outcomes: The primary outcome is the between-group difference of the Fugl-Meyer-Motor Assessment (FMMA) total score measured 3 months after randomization. Secondary outcomes include patient-reported health and wellbeing (PROMIS 10 and 29), patient-reported assessment of improvement, Rivermead Mobility Index, modified Rankin Scale, National Institutes of Health Stroke Scale (NIHSS), and as measures of harm: mortality, recurrent stroke, and serious adverse events.

Conclusion: The ESTREL trial will provide evidence of whether the use of Levodopa in addition to standardized rehabilitation in stroke patients leads to better functional recovery compared to rehabilitation alone.

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左旋多巴促进脑卒中康复(ESTREL):随机安慰剂对照双盲优效试验的原理与设计。
理由:中风康复需要新的治疗方法。药物疗法是否有利于促进中风的恢复尚不清楚。多巴胺是一种神经递质,参与运动学习、奖赏和大脑可塑性。其原药左旋多巴是一种有希望促进中风康复的药物:研究假设:与安慰剂相比,左旋多巴在基于主动任务训练的标准化康复治疗的基础上,可促进急性缺血性或出血性中风患者的功能恢复:ESTREL(左旋多巴促进中风康复)是一项随机(比例为 1:1)、多中心、安慰剂对照、双盲、平行组优效试验:610 名参与者(根据样本量计算)将在中风发作后⩽7 天内接受有临床意义的偏瘫治疗。主要资格标准包括:(i) 需要住院康复治疗;(ii) 有能力参加康复治疗;(iii) 以前日常生活自理:左旋多巴 100 毫克/卡比多巴 25 毫克,每日三次,持续 5 周,同时进行标准化康复治疗。研究干预将在中风发作后 7 天内开始:结果:主要结果是随机分组 3 个月后测量的 Fugl-Meyer-Motor Assessment(FMMA)总分的组间差异。次要结果包括患者报告的健康和幸福感(PROMIS 10 和 29)、患者报告的改善评估、Rivermead 活动指数、改良 Rankin 量表、美国国立卫生研究院卒中量表(NIHSS),以及作为危害度量的死亡率、复发性卒中和严重不良事件:ESTREL试验将为中风患者在标准化康复治疗的基础上使用左旋多巴是否会比单独使用康复治疗带来更好的功能恢复提供证据。
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来源期刊
CiteScore
7.50
自引率
6.60%
发文量
102
期刊介绍: Launched in 2016 the European Stroke Journal (ESJ) is the official journal of the European Stroke Organisation (ESO), a professional non-profit organization with over 1,400 individual members, and affiliations to numerous related national and international societies. ESJ covers clinical stroke research from all fields, including clinical trials, epidemiology, primary and secondary prevention, diagnosis, acute and post-acute management, guidelines, translation of experimental findings into clinical practice, rehabilitation, organisation of stroke care, and societal impact. It is open to authors from all relevant medical and health professions. Article types include review articles, original research, protocols, guidelines, editorials and letters to the Editor. Through ESJ, authors and researchers have gained a new platform for the rapid and professional publication of peer reviewed scientific material of the highest standards; publication in ESJ is highly competitive. The journal and its editorial team has developed excellent cooperation with sister organisations such as the World Stroke Organisation and the International Journal of Stroke, and the American Heart Organization/American Stroke Association and the journal Stroke. ESJ is fully peer-reviewed and is a member of the Committee on Publication Ethics (COPE). Issues are published 4 times a year (March, June, September and December) and articles are published OnlineFirst prior to issue publication.
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