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临床试验/NCT01737541
NCT01737541终止3 期

Fluoxetine for Motor Recovery After Acute Intracerebral Hemorrhage (FMRICH): a Randomised Placebo-controlled Trial

Universidad Autónoma de Aguascalientes4 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2012年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
终止
入组人数
32
试验地点
4
主要终点
Fugl Meyer Motor Scale score

研究概览

简要总结

This is a randomized, double-blind, placebo-controlled, multicenter clinical trial that will be carried out in Mexico. The purpose of this study is to test whether a 3-month treatment with fluoxetine enhances motor recovery in non-depressed patients with acute intracerebral hemorrhage.

详细描述

Spontaneous, nontraumatic intracerebral hemorrhage (ICH) is a subtype of stroke that causes a great amount of disability, economic and social burden. This is particularly true in developing countries where it accounts for between 20% and 50% of all strokes. Pharmacological and surgical interventions have been attempted to diminish the mortality and disability derived from ICH, with unsuccessful results. Recently the use of Fluoxetine in addition to physical rehabilitation has been proven useful to improve motor recovery from cerebral infarct. The purpose of this study is to test whether a 3-month treatment with fluoxetine enhances motor recovery in non-depressed patients with acute intracerebral hemorrhage.

This is a randomized, double-blind, placebo-controlled, multicenter clinical trial. This trial will recruit 86 patients with intracerebral hemorrhage of both sexes, ages >18 years, from four Mexican hospitals. The patients will receive either 20mg of fluoxetine or a placebo once daily for 90 days. The primary outcome is the mean change in Fugl-Meyer Motor Scale score between inclusion (day 0) and day 90. The secondary outcomes will be changes in Barthel Index, Modified Rankin scale and National Institutes of Health (NIH) Stroke Scale. The outcomes will be measured at day 45±7days and at day 90, for a total of four visits with each subject (at screening and at 0, 45 and 90days).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients who had an acute intracerebral hemorrhage within the past 10 days causing hemiparesis or hemiplegia
  • Fugl-Meyer motor scale (FMMS) scores of 55 or less
  • Written informed consent for participation in the trial

排除标准

  • Severe post-stroke disability (National Institutes of Health stroke scale [NIHSS] score >20)
  • Premorbid disability, evidenced by residual motor deficit from a previous stroke
  • Comprehension deficit or severe aphasia
  • Previous diagnosis of depression or one of the following:
  • Hospital Anxiety and Depression Scale score ≥11 points
  • Taking antidepressant drugs two weeks before inclusion
  • Taking neuroleptic drugs or benzodiazepines two weeks before inclusion
  • Other major diseases with life expectancy less than 3 months.

研究组 & 干预措施

Fluoxetine

Experimental

fluoxetine per os 20 mg daily

干预措施: Fluoxetine (Drug)

Placebo

Placebo Comparator

per os daily

干预措施: Placebo (Drug)

结局指标

主要结局

Fugl Meyer Motor Scale score

时间窗: Baseline and 90 days

Change from Baseline in Fugl Meyer Motor Scale score at 90 days

次要结局

  • NIH Stroke Scale(Baseline and 90 days)
  • Barthel Index(Baseline and 90 days)
  • modified Rankin Scale(Baseline and 90 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Juan Manuel Marquez-Romero

Profesor Investigador

Universidad Autónoma de Aguascalientes

研究点 (4)

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