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Effects of Botulinum Toxin Type A in Adults With Cerebral Palsy

Primary Purpose

Cerebral Palsy

Status
Completed
Phase
Phase 4
Locations
Norway
Study Type
Interventional
Intervention
Botulinum toxin type A (Botox)
placebo (saline)
Sponsored by
Sunnaas Rehabilitation Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cerebral Palsy focused on measuring Adult, Cerebral Palsy, Spastic contractures, Botulinum toxin type A

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Unilateral or bilateral spastic CP
  • Modified Ashworth Scale (MAS) ≥ 2 in ankle- or knee joint muscles.
  • ≥ 18 year of age, ≤ 65 year of age
  • Ambulant without walking aids minimum 10 metres in functional equines and/or with pathological knee extension or flexion pattern.

Exclusion Criteria:

  • Cognitive impairment.
  • No spasticity (MAS < 2 )
  • < 18 year of age
  • Not ambulant without walking aids
  • Pregnant or planning pregnancy
  • Btx-A treatment last 6 months
  • Orthopedic surgery lower extremity last 18 months
  • Obvious skeletal/joint deformity where orthopedic surgery is indicated
  • Other diseases which can affect level of function (rheumatoid or neurological )
  • New treatment the past four weeks which affect the musculoskeletal system (pain killers, physical therapy, acupuncture)

Sites / Locations

  • Sunnaas Rehabilitation Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

I

II

Arm Description

Botox

Outcomes

Primary Outcome Measures

Ankle sagittal kinematic with corresponding knee and hip data (3D-gait analysis)
Summary measure of health related quality of life (SF-36)

Secondary Outcome Measures

Stiffness/spasticity according to VAS
Questionnaire gait function
Spasticity in ankle, knee and hip according to Modified Ashworth Scale
3D-gait data (Kinetics,Temporospatial (stride length, velocity)
Global Scale
Timed Up and Go
6 minutes walking test
Registrations of sample characteristics
Registration of adverse reactions
Pain according to VAS

Full Information

First Posted
February 5, 2007
Last Updated
February 23, 2009
Sponsor
Sunnaas Rehabilitation Hospital
Collaborators
The Royal Norwegian Ministry of Health
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1. Study Identification

Unique Protocol Identification Number
NCT00432055
Brief Title
Effects of Botulinum Toxin Type A in Adults With Cerebral Palsy
Official Title
A Randomized Controlled Trial on Effects of Botulinum Toxin Type A in Adults With Cerebral Palsy
Study Type
Interventional

2. Study Status

Record Verification Date
February 2009
Overall Recruitment Status
Completed
Study Start Date
January 2007 (undefined)
Primary Completion Date
January 2009 (Actual)
Study Completion Date
January 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Sunnaas Rehabilitation Hospital
Collaborators
The Royal Norwegian Ministry of Health

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this project is to investigate if there is a significant difference in active joint range of motion, questionnaire on gait function and health related quality of life between patients randomized to treatment with Botulinum toxin type A and patients randomized to placebo treatment.
Detailed Description
Cerebral palsy (CP) is a constellation of symptoms and conditions defined as lifelong motor dysfunction resulting rom a non-progressive brain lesion occurring pre-, peri- or postnatal before the second year of life. CP consists of different aspect of motor disorder including spasticity, paresis, incoordination and dystonia There is scarce knowledge about the association between spasticity, pain and physical function in the adult CP-population, and the systematic follow up of patients with CP typically ends at the age of eighteen. Frequently used intervention in spastic cerebral palsy for children with gait problems are injections with Botulinum toxin type A (Btx-A) in leg and thigh muscles, and three dimensional-gait analysis has become a standard procedure in treatment decision and evaluation. Botulinum toxin A (Btx- A) is a highly effective treatment in the management of spasticity. The first reported success of use of Btx-A in children with cerebral palsy was made in 1993 by Koman et al. Subsequently, randomized controlled studies on children with spastic type of cerebral palsy has documented that Btx-A is effective and safe in the management of muscle spasticity in children with CP. There is an implicit, and as of yet, unproven assumption that there is no indication for this treatment in the adult CP-population.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Palsy
Keywords
Adult, Cerebral Palsy, Spastic contractures, Botulinum toxin type A

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
66 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
I
Arm Type
Experimental
Arm Description
Botox
Arm Title
II
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Botulinum toxin type A (Botox)
Intervention Type
Drug
Intervention Name(s)
placebo (saline)
Primary Outcome Measure Information:
Title
Ankle sagittal kinematic with corresponding knee and hip data (3D-gait analysis)
Time Frame
8 week
Title
Summary measure of health related quality of life (SF-36)
Time Frame
8 week , 16 week
Secondary Outcome Measure Information:
Title
Stiffness/spasticity according to VAS
Time Frame
8 week, 16 week
Title
Questionnaire gait function
Time Frame
8 week, 16 week
Title
Spasticity in ankle, knee and hip according to Modified Ashworth Scale
Time Frame
8 week,
Title
3D-gait data (Kinetics,Temporospatial (stride length, velocity)
Time Frame
8 week
Title
Global Scale
Time Frame
8 week, 16 week
Title
Timed Up and Go
Time Frame
8 week
Title
6 minutes walking test
Time Frame
8 week
Title
Registrations of sample characteristics
Time Frame
0 week
Title
Registration of adverse reactions
Time Frame
8 week, 16 week
Title
Pain according to VAS
Time Frame
8 week, 16 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Unilateral or bilateral spastic CP Modified Ashworth Scale (MAS) ≥ 2 in ankle- or knee joint muscles. ≥ 18 year of age, ≤ 65 year of age Ambulant without walking aids minimum 10 metres in functional equines and/or with pathological knee extension or flexion pattern. Exclusion Criteria: Cognitive impairment. No spasticity (MAS < 2 ) < 18 year of age Not ambulant without walking aids Pregnant or planning pregnancy Btx-A treatment last 6 months Orthopedic surgery lower extremity last 18 months Obvious skeletal/joint deformity where orthopedic surgery is indicated Other diseases which can affect level of function (rheumatoid or neurological ) New treatment the past four weeks which affect the musculoskeletal system (pain killers, physical therapy, acupuncture)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Johan K Stanghelle, Professor MD
Organizational Affiliation
Research Departement, Sunnaas Rehabilitation Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Sunnaas Rehabilitation Hospital
City
Bjoernemyr
State/Province
Nesoddtangen
ZIP/Postal Code
1450
Country
Norway

12. IPD Sharing Statement

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Effects of Botulinum Toxin Type A in Adults With Cerebral Palsy

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