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Improvement After Botulinum Toxin Injections to the Arms in Children With Cerebral Palsy

Primary Purpose

Cerebral Palsy

Status
Terminated
Phase
Phase 4
Locations
Israel
Study Type
Interventional
Intervention
physiotherapy
Botulinum Toxin A and physiotherapy
Sponsored by
Shaare Zedek Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cerebral Palsy focused on measuring children with cerebral palsy ages eight to eleven.

Eligibility Criteria

8 Years - 11 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • cooperative quadriplegic CP children
  • gross motor function level 4
  • troublesome hypertonia that will respond to treatment with Botox

Exclusion Criteria:

  • cognitive impairment (IQ<70)
  • severe behavioural disorder

Sites / Locations

  • Shaare Zedek Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

BG

Control Group

Arm Description

cooperative quadriplegic CP children ages 8-11 years, gross motor function level 4 with troublesome hypertonia that will respond to treatment. BG children will be given Botulinum Toxin A, as clinically required, in addition to an equivalent program of intensive therapy

control group: Twenty cooperative quadriplegic CP children ages 8-11 years, gross motor function level 4 with troublesome hypertonia that will respond to treatment.CG children will undergo a program of intensive therapy.

Outcomes

Primary Outcome Measures

Quality of life

Secondary Outcome Measures

1. Hypertonia 2. Impairment measures 3. Upper extremity function 4. Function and patient needs assessment

Full Information

First Posted
October 24, 2007
Last Updated
April 20, 2011
Sponsor
Shaare Zedek Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT00549471
Brief Title
Improvement After Botulinum Toxin Injections to the Arms in Children With Cerebral Palsy
Official Title
Improvement After Botulinum Toxin A Injections to the Upper Extremities in Children With Cerebral Palsy
Study Type
Interventional

2. Study Status

Record Verification Date
April 2011
Overall Recruitment Status
Terminated
Why Stopped
no funding
Study Start Date
September 2007 (undefined)
Primary Completion Date
September 2012 (Anticipated)
Study Completion Date
September 2012 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Shaare Zedek Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Hypothesis: (1) Treating upper limb hypertonia/spasticity with Botox®, in addition to reducing hypertonia/spasticity, will (a) improve global development, (b) improve function (passive & active), (c) reduce carer burden and (d) improve quality of life. (2) Early treatment with Botox® will have a greater impact on the rate of global development when compared to late treatment.
Detailed Description
Background: Upper limb function is essential for activities of daily living impacting on quality of life in children with cerebral palsy (CP). In preschool children, dysfunctional upper extremity manipulation not only leads to disability but may further delay global development and substantially increase career burden. Even modest functional improvement could have tremendous long-term benefit in activities of daily living and significantly reduce career burden. Hypertonia is the main symptom causing motor dysfunction in CP. Intramuscular Botulinum toxin injection is one way of treatment. In spite of anecdotal evidence suggesting that early intervention can lead to better outcomes, Israeli physicians are unable to prescribe this treatment for the upper extremities due to limited health insurance coverage. A paucity research evidence is often cited as the reason for limiting the insurance coverage, in particular to the upper limb. We therefore propose to study the effects of Botox® in treating children with CP. Method: Twenty cooperative quadriplegic CP children ages 8-11 years, gross motor function level 4, will be enrolled for the study. Inclusion criteria will be troublesome hypertonia that will respond to treatment with Botox® (as identified by clinical assessment and neurophysiological measures). Since cooperation is crucial for the intensive therapy children with cognitive impairment (IQ<70) or severe behavioural disorders will be excluded. The children will be randomized to one of two groups a Botox group (BG) and a control group (CG). CG children will undergo a program of intensive therapy and BG children will be given Botox, as clinically required, in addition to an equivalent program of intensive therapy. Botox injection will be tailored according to the specific child. Generally injection site will include biceps and brachioradialis , while flexors of the wrist and digits will be injected according to abnormal postures during function. Maximal total dose will be 23 IU per kg. The intensive therapy will be as clinically required and the therapy program will be fully documented. Outcome measures will include the following: Hypertonia- neurophysiological measures Impairment measures - Grip and Pinch strength, active and passive range of motion at the writs elbow and shoulder Upper extremity function - Quality of Upper Extremity Skills Test (QUEST), Box and Blocks test Function and patient needs assessment - Goal Attainment Scores, Developmental Fine Motor Scale, Pediatric Evaluation and Disability Inventory (PEDI) Quality of life scales (care and comfort hypertonicity questionnaire) All of these measures will be taken once before treatment and then repeated at 7 months, and at 13 months after treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Palsy
Keywords
children with cerebral palsy ages eight to eleven.

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
3 (Actual)

8. Arms, Groups, and Interventions

Arm Title
BG
Arm Type
Experimental
Arm Description
cooperative quadriplegic CP children ages 8-11 years, gross motor function level 4 with troublesome hypertonia that will respond to treatment. BG children will be given Botulinum Toxin A, as clinically required, in addition to an equivalent program of intensive therapy
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
control group: Twenty cooperative quadriplegic CP children ages 8-11 years, gross motor function level 4 with troublesome hypertonia that will respond to treatment.CG children will undergo a program of intensive therapy.
Intervention Type
Other
Intervention Name(s)
physiotherapy
Intervention Description
CG children will undergo a program of intensive physiotherapy
Intervention Type
Other
Intervention Name(s)
Botulinum Toxin A and physiotherapy
Intervention Description
BG children will be given Botox, as clinically required, in addition to an equivalent program of intensive therapy. Botox injection will be tailored according to the specific child. Generally injection site will include biceps and brachioradialis, while flexors of the wrist and digits will be injected according to abnormal postures during function. Maximal total dose will be 23 IU per kg.
Primary Outcome Measure Information:
Title
Quality of life
Time Frame
2 years
Secondary Outcome Measure Information:
Title
1. Hypertonia 2. Impairment measures 3. Upper extremity function 4. Function and patient needs assessment
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
11 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: cooperative quadriplegic CP children gross motor function level 4 troublesome hypertonia that will respond to treatment with Botox Exclusion Criteria: cognitive impairment (IQ<70) severe behavioural disorder
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hilla Ben-Pazi, MD
Organizational Affiliation
Shaare Zedek Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Shaare Zedek Medical Center
City
Jerusalem
ZIP/Postal Code
91031
Country
Israel

12. IPD Sharing Statement

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Improvement After Botulinum Toxin Injections to the Arms in Children With Cerebral Palsy

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