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Botulinum Toxin (BOTOX) for Cerebral Palsy - Article


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Cerebral Gigantism

 




Clinical Trial: Botulinum Toxin (BOTOX) for Cerebral Palsy

This study is no longer recruiting patients.

Sponsored by: National Institute of Child Health and Human Development (NICHD)
Information provided by: National Institute of Child Health and Human Development (NICHD)

Purpose

This study examines botulinum toxin (BOTOX, or BTX) for the treatment of muscle twitches and spasticity associated with cerebral palsy in children. Botulinum toxin is a naturally occurring bacterial toxin (botulinum toxin) that inactivates certain parts of muscles.

Condition Treatment or Intervention Phase
Cerebral Palsy
Muscle Spasticity
 Drug: Botulinum toxin type A
Phase II

MedlinePlus related topics:  Cerebral Palsy;   Neuromuscular Disorders

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study

Official Title: Botulinum Toxin for Spasticity in Cerebral Palsy

Further Study Details: 

Expected Total Enrollment:  40

Study start: July 1997;  Study completion: June 2002

This trial will test the effectiveness of BTX injections versus placebo to reduce plantar-flexor spasticity and improve function and mobility in children with spastic diplegia, a common form of cerebral palsy. The study will evaluate the effects of the treatment across five domains that relate to disability: pathophysiology, impairment, functional limitation, disability, and societal limitation.

Forty children, ages 4 to 12 years, will be recruited and randomized into one of two groups. Group A will receive BTX. Group B will receive a placebo injection. Participants will be assessed at the beginning of the trial and at Weeks 3, 8, 12, and 24. Assessments include quantitative electromyographic kinesiology measurements, electromechanical measurement of joint torque across the ankle joint using the Spasticity Measurement System, Gross Motor Function Measure, physical exam parameters, energy expenditure using the Energy Cost Index, kinematic gait analysis, and the Canadian Occupational Performance Measure.

Participants are followed for a total of 6 months. Participants initially randomized to Group B will have the opportunity for BTX treatment after 24 weeks.

Eligibility

Ages Eligible for Study:  3 Years   -   12 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

  • Spastic diplegic cerebral palsy
  • Community or independent ambulators
  • Expressive communication skills at age 3 or above
  • Stable social environment
  • Reasonable proximity to the medical center
  • Physical therapy at least once per week
  • No other serious health problems that would interfere with the study

Exclusion Criteria:

  • Other forms of cerebral palsy
  • Previous treatment with botulinum toxin
  • Musculoskeletal contractures greater than 15 degrees
  • Unstable social environment

Location Information


Washington
      Children's Hospital and Regional Medical Center, Seattle,  Washington,  98105,  United States

Study chairs or principal investigators

Ross M. Hays, M.D.,  Principal Investigator,  Children's Hospital and Regional Medical Center   

More Information

Study ID Numbers:  1R01HD35750-01
Record last reviewed:  October 2004
Last Updated:  October 13, 2004
Record first received:  May 16, 2003
ClinicalTrials.gov Identifier:  NCT00060957
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 8, 2005

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November 29, 2009



Page Updated: September 6, 2005
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