Trial of Ropinirole in Motor Recovery After Stroke
Information source: University of California, Irvine
Information obtained from ClinicalTrials.gov on June 20, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Cerebrovascular Accident; Hemiparesis
Intervention: Ropinirole (+ physical therapy) (Drug); (vs.) Placebo + physical therapy (Drug)
Phase: Phase 2
Status: Completed
Sponsored by: University of California, Irvine Official(s) and/or principal investigator(s): Steven C Cramer, MD, Principal Investigator, Affiliation: University of California, Irvine
Summary
The purpose of this study is to assess efficacy, as well as safety, of Ropinirole in
improving movement among patients with chronic stroke.
Clinical Details
Official title: Randomized, Placebo-Controlled, Double-Blind Pilot Trial to Evaluate the Safety and Efficacy of Ropinirole in Motor Recovery After Stroke
Study design: Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Safety/Efficacy Study
Secondary outcome: Barthel IndexLeg motor Fugl-Meyer scale Stroke Impact Scale-16 Gait endurance Hamilton Depression Scale Safety
Detailed description:
Stroke is a leading cause of disability. Current treatments target injury and must be
delivered within hours. A body of literature suggests that there are processes ongoing
days-months after stroke that can be targeted therapeutically, and improve function. The
current study evaluates one such potential therapy, the dopamine agonist ropinirole. The
current study tests the hypothesis that patients with chronic stroke randomized to
ropinirole+physiotherapy will show improved gait velocity over the 12 weeks of study
participation as compared to patients randomized to placebo+physiotherapy. A secondary aim
is to test the hypothesis that ropinirole will improve three secondary endpoints at 12 weeks
after study entry: the proportion of patients with no significant disability (Barthel Index
≥ 95); overall motor status, measured with the arm/leg FM score; and overall physical
function, defined as the score on the Stroke Impact Scale-16 (SIS-16). This study will also
evaluate the safety of ropinirole in patients recovering from stroke.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
1. Stroke onset 4 weeks-12 months prior
2. Stroke is radiologically confirmed as either (a) ischemic or (b) hemorrhagic
3. Minimum age 18
4. No significant pre-stroke disability
5. No other stroke in previous 3 months
6. Absence of major depression
7. Fugl-Meyer (FM) motor score of 23-83 out of 100
8. Functional Independence Measure (FIM) ambulation-subscore of 3 or more, and 50 foot
walk takes longer than 15 seconds
Exclusion Criteria:
1. Significant daytime somnolence or any substantial decrease in alertness, language
reception, or attention
2. Pregnant or lactating
3. Advanced liver, kidney, cardiac, or pulmonary disease
4. Orthostatic hypotension
5. Current use of ciprofloxacin, a centrally acting dopamine agonist, or a centrally
active dopamine antagonist
6. A terminal medical diagnosis consistent with survival < 1 year
7. Coexistent major neurological disease
8. Coexistent major psychiatric disease
9. A history of significant alcohol or drug abuse in the prior 3 years
10. A coexistent disease characterized by an abnormality of CNS dopaminergic tone
11. Current enrollment in another investigational study related to stroke or stroke
recovery
12. Contraindication to ropinirole prescription
Locations and Contacts
University of California, Irvine, Irvine, California 92697-1385, United States
Additional Information
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Starting date: October 2003
Ending date: May 2007
Last updated: January 25, 2008
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