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Clinical Trials/EUCTR2004-002427-40-GB
EUCTR2004-002427-40-GB
Active, not recruiting
Phase 1

What is the clinical effect and cost effectiveness of treating upper limb spasticity due to stroke with botulinum toxin?

ewcastle Upon Tyne Hospitals NHS Foundation Trust0 sites332 target enrollmentJuly 19, 2005

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
pper limb spasticity following stroke
Sponsor
ewcastle Upon Tyne Hospitals NHS Foundation Trust
Enrollment
332
Status
Active, not recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 19, 2005
End Date
February 28, 2009
Last Updated
6 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
ewcastle Upon Tyne Hospitals NHS Foundation Trust

Eligibility Criteria

Inclusion Criteria

  • Aged over 18 years
  • At least 1 month since stroke
  • Upper limb spasticity ( MAS \>2 at the elbow and/or spasticity at wrist or shoulder (no validated measure of spasticity at these sites.)
  • Reduced UL function (ARAT score 0\-56\).
  • Willing and able to participate in UL therapy programme.
  • Patient must be able and willing to understand and comply with the requirements of the protocol and the UL therapy programme.
  • Written informed consent before completing any study\-related procedure (any assessment or evaluation that would not have formed par of their normal care). Patient must be able and willing to understand and comply with the requirements of the protocol and the UL therapy programme.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes

Exclusion Criteria

  • Significant speech or cognitive impairment which will impede assessment
  • Other significant upper limb impairment e.g. fracture or frozen shoulder within 6 months, severe arthritis, amputation.
  • Evidence of contracture
  • Pregnancy or lactation (female patients who are at risk of pregnancy must have a negative pregnancy test on the day of randomisation and prior to any subsequent botulinum injection).
  • Female patients at risk of pregnancy who are not willing to take adequate precautions against pregnancy for the duration of the study.
  • Diagnosis likely to interfere with rehabilitation or outcome assessments e.g. registered blind, malignancy.
  • Other diagnosis which may contribute to upper limb spasticity e.g. multiple sclerosis, cerebral palsy.
  • Contraindications to intramuscular injection.
  • Religious objections to blood products(botulinum toxin contains human albumin)
  • Contraindications to botulinum toxin which include bleeding disorders, myasthenia gravis and concurrent use of aminoglycosides.

Outcomes

Primary Outcomes

Not specified

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