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Fluoxetine on Motor Rehabilitation After Ischemic Stroke (FLAME)
This study is ongoing, but not recruiting participants.
Study NCT00657163   Information provided by University Hospital, Toulouse
First Received: April 8, 2008   Last Updated: July 16, 2009   History of Changes

April 8, 2008
July 16, 2009
March 2005
December 2009   (final data collection date for primary outcome measure)
Progression in the Fugl-Meyer Motor Scale [ Time Frame: M3 (3 months) ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00657163 on ClinicalTrials.gov Archive Site
  • Fugl-Meyer Stroke Scale [ Time Frame: M12 (12 months) ] [ Designated as safety issue: No ]
  • NIH stroke scale [ Time Frame: M3 and M12 ] [ Designated as safety issue: No ]
  • MADRS depression scale [ Time Frame: M3 and M12 ] [ Designated as safety issue: No ]
  • Modified Rankin scale [ Time Frame: M3 and M12 ] [ Designated as safety issue: No ]
  • Mortality [ Time Frame: M3 and M12 ] [ Designated as safety issue: Yes ]
Same as current
 
Fluoxetine on Motor Rehabilitation After Ischemic Stroke
Effects of 3 Months Daily Treatment With Selective Serotonin Reuptake Inhibitor (SSRI, Fluoxetine) on Motor Rehabilitation After Ischemic Stroke. FLAME Trial

Recovery from stroke is a major process and, except for acute intravenous thrombolysis, no treatment able to enhance recovery has yet been validated. Some drugs may have a positive effect when combined with physical rehabilitation. Previous studies have shown a potential effect of catecholaminergic drugs on cerebral plasticity of stroke patients. In 2001, our group has demonstrated in a small group of stroke patients (n=8) that a single dose of fluoxetine (Selective Serotonin Reuptake Inhibitor - SSRI) improved motor performance and modulated cerebral plasticity. We conducted a phase IIb prospective, double-blind, randomized, placebo controlled study to assess the effect of a daily treatment with fluoxetin (20 mg) on motor performance in patients with mild to severe motor deficit after ischemic stroke.

We project to include in the study a maximum of 168 patients with a recent (5 to 10 days) ischemic stroke and unilateral motor deficit in order to obtain 100 completed patients. Nine stroke centers in France are involved.

Each patient will receive daily, during three months, 20 mg of fluoxetin or placebo.

Patients will be evaluated at inclusion, day 30, M3 (3 months), M12.

Phase II
Interventional
Treatment, Randomized, Double Blind (Subject, Investigator), Parallel Assignment, Safety/Efficacy Study
  • Ischemic Stroke
  • Motor Impairment
  • Drug: fluoxetine
  • Drug: placebo
  • Experimental: fluoxetine
  • Placebo Comparator: Placebo

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Active, not recruiting
100
June 2010
December 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Men and women aged from 18 to 85
  • No motor relapse from a previous stroke
  • Inclusion from day 5 to day 10 after stroke
  • Ischemic stroke with unilateral motor deficit
  • Motor NIHSS ≥ 5 on the affected side of the body
  • NIHSS < 20
  • Fugl Meyer Motor Scale <55
  • Modified Rankin Scale between 1 and 5
  • Informed consent obtained from the subject or a member of his family

Exclusion Criteria:

  • Pregnant or breast-feeding woman
  • Woman able to procreate without valid contraception
  • Subject protected by law
  • Concomitant disease with unfavourable prognosis within 1 year
  • Drug addiction
  • Allergy to fluoxetine
  • Hepatic failure (TGO and TGP >2N)
  • Permanent Renal failure (Creatinin >180micromol/l)
  • Patients treated by tricyclic antidepressant, selective serotonin reuptake inhibitor, monoamine oxidase inhibitor (IMAO), and neuroleptics in the past month
  • Depression requiring pharmacological treatment
  • Previous stroke with motor relapse
  • Fugl Meyer Motor Scale > 55
  • Modified Rankin Scale = 0 or 6
  • Patients needing carotid surgery within 3 months
  • Aphasia preventing correct evaluation of motor and depression scales.
Both
18 Years to 85 Years
No
Contact information is only displayed when the study is recruiting subjects
France
 
NCT00657163
LLAU Marie-Elise, University Hospital Toulouse
0300501, French PHRC
University Hospital, Toulouse
 
Principal Investigator: François Chollet, PhD University Hospital, Toulouse
University Hospital, Toulouse
July 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP