Dopamine Treatment in Children With Cerebral Palsy With Dystonia- A Double Blind Controlled Study
Primary Purpose
Dystonic Cerebral Palsy
Status
Unknown status
Phase
Phase 4
Locations
Israel
Study Type
Interventional
Intervention
L- DOPA
placebo
Sponsored by
About this trial
This is an interventional treatment trial for Dystonic Cerebral Palsy
Eligibility Criteria
Inclusion Criteria:
- clear pathophysiological cause for CP
- disabling dystonia in upper limbs
Exclusion Criteria:
- significant contractures
- psychiatric disorder
Sites / Locations
- Shaare Zedek Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
DOPAMINE
Placebo
Arm Description
Sinemet up to 10 mg/kg/day
placebo
Outcomes
Primary Outcome Measures
QUEST quality of upper extremity skills test score before and after treatment
The QUEST is a measure designed to evaluate movement patterns and hand function in children with cerebral palsy. It is administered within a play context. Items are related to quality of movement, not to chronological age. There are 36 items assessing dissociated movements, grasp, protective extension, and weight bearing.
Secondary Outcome Measures
box and blocks, 9 hole pegs, pronation/ supination, finger sequencing
Difference between test scores before and after treatment. Namely:
of box transfered per minute time to complete the 9 hole pegs insertion.
pronation/ supination per 20 seconds time to complete 5 finger sequencing rounds
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01361373
Brief Title
Dopamine Treatment in Children With Cerebral Palsy With Dystonia- A Double Blind Controlled Study
Study Type
Interventional
2. Study Status
Record Verification Date
May 2011
Overall Recruitment Status
Unknown status
Study Start Date
May 2010 (undefined)
Primary Completion Date
May 2012 (Anticipated)
Study Completion Date
August 2012 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Shaare Zedek Medical Center
4. Oversight
5. Study Description
Brief Summary
Background:
Cerebral palsy (CP) is the main cause of childhood immobility and is defined as a non progressive injury to the developing central nervous system in children younger than 3 years, resulting in neurological and musculoskeletal abnormalities. The main pathophysiological causes are encephalopathy of prematurity (periventricular leukomalacia) hypoxic ischemic encephalopathy. Infections, infracts and migration defects are other less common causes of CP. The brain injury leads to functional motor impairment impacting on daily activities commonly manifests as a movement disorder: pyramidal, leading to spasticity and extra-pyramidal leading to dystonia and chorea. In most cases extensive brain injury causes a mixed movement disorder. Dystonia is defined as involuntary muscle contractions causing twisting and abnormal postures. While the neurological underpinnings of CP remain unknown, a link between low dopamine and increased acetylcholine release has recently been reported in dystonia. Dopamine is considered the first line of treatment in children with dystonia and CP followed by anticholiergic treatment with trihexphenidyl. The recommendation of dopaminergic treatment is based on need to rule out dopamine-responsive-dystonia, a rare genetic disorder, and on single case study reporting improvement in CP. A double blind study support or refute the use of dopamine treatment for dystonic CP was never reported. Working hypothesis and
Aims:
In children with CP due to a clear underlying pathology, dopamine treatment will not improve daily function. Methods: the investigators will perform a double blinded randomized controlled crossover study. 50 children ages 4-18 years with a clear pathophysiological cause for CP will be enrolled. Each child will receive dopamine and placebo treatment for 2 weeks with a 2 week washout interval. Participants will be randomized into 2 groups; one will receive placebo followed by dopamine and the other vice versa. The primary outcome measure, goal-attainment-scale, and secondary outcome functional measures (such as box and blocks, 9 hole pegs, pronation/ supination, finger sequencing) will be assessed at the beginning and end of each treatment as well as parent questionnaires regarding satisfaction and side effects.
Expected results:
No functional improvement with dopamine treatment compared to placebo.
Importance:
supplying sufficient data to support or refute the use of dopamine treatment for dystonic CP.
Probable implications to Medicine:
this may lead to a change in medical treatment guidelines for children with CP.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dystonic Cerebral Palsy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
DOPAMINE
Arm Type
Active Comparator
Arm Description
Sinemet up to 10 mg/kg/day
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
placebo
Intervention Type
Drug
Intervention Name(s)
L- DOPA
Intervention Description
Sinemet up to 10 mg/kg/ day increasing gradually for 2 weeks
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
placebo for 2 weeks
Primary Outcome Measure Information:
Title
QUEST quality of upper extremity skills test score before and after treatment
Description
The QUEST is a measure designed to evaluate movement patterns and hand function in children with cerebral palsy. It is administered within a play context. Items are related to quality of movement, not to chronological age. There are 36 items assessing dissociated movements, grasp, protective extension, and weight bearing.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
box and blocks, 9 hole pegs, pronation/ supination, finger sequencing
Description
Difference between test scores before and after treatment. Namely:
of box transfered per minute time to complete the 9 hole pegs insertion.
pronation/ supination per 20 seconds time to complete 5 finger sequencing rounds
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
clear pathophysiological cause for CP
disabling dystonia in upper limbs
Exclusion Criteria:
significant contractures
psychiatric disorder
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hilla Ben- Pazi, MD
Email
Benpazi@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Hilla Ben- Pazi
Email
Benpazi@gmail.com
Facility Information:
Facility Name
Shaare Zedek Medical Center
City
Jerusalem
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hilla Ben- Pazi, MD
Email
Benpazi@gmail.com
12. IPD Sharing Statement
Citations:
PubMed Identifier
23349519
Citation
Pozin I, Bdolah-Abram T, Ben-Pazi H. Levodopa does not improve function in individuals with dystonic cerebral palsy. J Child Neurol. 2014 Apr;29(4):534-7. doi: 10.1177/0883073812473645. Epub 2013 Jan 24.
Results Reference
derived
Learn more about this trial
Dopamine Treatment in Children With Cerebral Palsy With Dystonia- A Double Blind Controlled Study
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