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临床试验/NCT01129479
NCT01129479已完成不适用

Galantamine Treatment for Nonfluent Aphasia in Stroke Patients

University of North Carolina, Chapel Hill0 个研究点目标入组 8 人开始时间: 2004年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
8
主要终点
Spontaneous Speech

研究概览

简要总结

Cognitive impairment after stroke is common and has a major effect on morbidity and quality of life. Acetylcholinesterase inhibitors have demonstrated benefit in vascular dementia, but efficacy in treating more circumscribed cognitive deficits following stroke, such as aphasia, has not been systematically investigated.

This study evaluated the efficacy of Galantamine (Reminyl) in subjects with chronic, stable non-fluent aphasia secondary to stroke. Subjects enrolled in a double-blind placebo- controlled cross-over study that employed a comprehensive battery of language tests and measures of general cognitive and behavioral status that will be used to control for factors that may influence language functioning. The primary study outcome was a within-subject comparison of changes in language function and behavioral scores between placebo and active-treatment phases (12 weeks each). Our hypothesis was that by increasing acetylcholine levels, and facilitating activity of other neurotransmitters affecting attentional systems, Galantamine would produce gains in both language and behavioral scores in patients suffering chronic effects in cognitive systems due to injury following stroke.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
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

  • Diagnosis of aphasia with relatively spared comprehension.
  • Onset 6 months or greater prior to enrollment.
  • Native English speaker
  • Right-handed.
  • Adults (18 years of age or older).

排除标准

  • Patients receiving ongoing individual speech therapy. (Most patients are no longer eligible for individualized speech therapy after 6 months from stroke onset, thus this should not eliminate many patients).
  • Extremely mild or extremely severe aphasia. (Boston Naming Test Score <3 or >45 items named from 60 items).
  • Global dementia (and any other patient with reduced decisional capacity requiring a legally authorized representative for consent).
  • Presence of major cognitive deficit other than aphasia caused by stroke related disease.
  • Contraindications to cholinomimetic agents: History of active peptic ulcer disease within 1 year, Severe asthma, unstable angina, bradyarrhythmia with resting pulse less than 50, sick sinus syndrome, or seizures.
  • Major psychiatric disorders that affect cognition including: psychosis, major depression, bipolar disorder, alcohol or substance abuse.
  • Major medical conditions that alter cognition (e.g., heart failure, dialysis dependent renal failure, hepatic failure, active cancer).
  • Impairments that affect metabolism of the medication including: Severe renal impairment (Creatinine clearance equal to or greater than 9), and moderate or severe hepatic impairment (Child-Pugh score >7)
  • Patients using medications that have major effects on brain neurotransmitter systems or cognition within 2 months of enrollment. Exclusionary medications are: medications with significant anti-cholinergic activity (tricyclic antidepressants, diphenhydramine), anti-Parkinsonian medications (including Sinemet, amantadine, bromocriptine, pergolide, selegiline), and narcotic analgesics (> 2 doses per week).

研究组 & 干预措施

Galantamine

Active Comparator

干预措施: Galantamine (Drug)

Placebo

Placebo Comparator

干预措施: Placebo pill (Drug)

结局指标

主要结局

Spontaneous Speech

时间窗: Every 4 weeks

Analysis of spontaneous speech production with picture description (cookie theft picture): content units and lexical efficiency; as well as Boston Naming Test naming latency.

次要结局

  • ADP(Every 4 weeks)
  • Communication Log scores(Every 12 weeks)

研究者

申办方类型
Other

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