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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
Shaare Zedek Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dystonic Cerebral Palsy

Eligibility Criteria

4 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

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

First Posted
June 6, 2010
Last Updated
May 26, 2011
Sponsor
Shaare Zedek Medical Center
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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

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Dopamine Treatment in Children With Cerebral Palsy With Dystonia- A Double Blind Controlled Study

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