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Completed

NCT Number: NCT00221390

Trial of Ropinirole in Motor Recovery After Stroke

The purpose of this study is to assess efficacy, as well as safety, of Ropinirole in improving movement among patients with chronic stroke.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

University of California, Irvine Medical Center

Orange, California, 92868, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Stroke onset 4 weeks-12 months prior
  • Stroke is radiologically confirmed as either (a) ischemic or (b) hemorrhagic
  • Minimum age 18
  • No significant pre-stroke disability
  • No other stroke in previous 3 months
  • Absence of major depression
  • Fugl-Meyer (FM) motor score of 23-83 out of 100
  • Functional Independence Measure (FIM) ambulation-subscore of 3 or more, and 50 foot walk takes longer than 15 seconds

Exclusion criteria

  • Significant daytime somnolence or any substantial decrease in alertness, language reception, or attention
  • Pregnant or lactating
  • Advanced liver, kidney, cardiac, or pulmonary disease
  • Orthostatic hypotension
  • Current use of ciprofloxacin, a centrally acting dopamine agonist, or a centrally active dopamine antagonist
  • A terminal medical diagnosis consistent with survival < 1 year
  • Coexistent major neurological disease
  • Coexistent major psychiatric disease
  • A history of significant alcohol or drug abuse in the prior 3 years
  • A coexistent disease characterized by an abnormality of CNS dopaminergic tone
  • Current enrollment in another investigational study related to stroke or stroke recovery
  • Contraindication to ropinirole prescription

Treatment and study plan

Ropinirole (+ physical therapy)

Drug

(vs.) Placebo + physical therapy

Drug

Secondary outcomes

  1. Barthel Index

    Time frame: Measured at weeks 1, 9, and 12

  2. Leg motor Fugl-Meyer scale

    Time frame: Measured at baseline and weeks 1, 2, 4, 6, 7, 8, 9, and 12

  3. Stroke Impact Scale-16

    Time frame: Measured at weeks 1, 4, 7, 9, and 12

  4. Gait endurance

    Time frame: Measured at weeks 1, 2, 4, 6, 7, 8, 9, and 12

  5. Hamilton Depression Scale

    Time frame: Measured at baseline and weeks 1, 2, 9, and 12

  6. Safety

    Time frame: 12 weeks

Sponsors and collaborators

Lead sponsor

University of California, Irvine

Other

Collaborators

  • GlaxoSmithKline

Registry information

Official study title

Randomized, Placebo-controlled, Double-blind Pilot Trial to Evaluate the Safety and Efficacy of Ropinirole in Motor Recovery After Stroke

Important dates

Study start
2003
Primary completion
2007
Study completion
2007
First posted
Sep 22, 2005
Registry last updated
Nov 1, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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