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Does Oral Baclofen Improve Care and Comfort in Spastic Children in Nursing Homes?

Primary Purpose

Cerebral Palsy

Status
Terminated
Phase
Phase 4
Locations
Israel
Study Type
Interventional
Intervention
oral baclofen + placebo
placebo + oral baclofen
Sponsored by
Shaare Zedek Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Cerebral Palsy focused on measuring nursing homes, children, ages 1-18 years, spastic quadriplegia

Eligibility Criteria

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

Inclusion Criteria:

  • Cerebral palsy nursing homes children ages 1-18 years spastic quadriplegia

Exclusion Criteria:

  • active epilepsy severe truncal hypotonia

Sites / Locations

  • Saare Zedek Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

group a

group b

Arm Description

Baclofen followed by Placebo

Placebo followed by Baclofen

Outcomes

Primary Outcome Measures

care and comport questionnaires

Secondary Outcome Measures

Full Information

First Posted
September 15, 2008
Last Updated
December 27, 2018
Sponsor
Shaare Zedek Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT00752934
Brief Title
Does Oral Baclofen Improve Care and Comfort in Spastic Children in Nursing Homes?
Study Type
Interventional

2. Study Status

Record Verification Date
December 2018
Overall Recruitment Status
Terminated
Why Stopped
Lack of funding
Study Start Date
October 2010 (undefined)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
June 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shaare Zedek Medical Center

4. Oversight

5. Study Description

Brief Summary
Baclofen is a drug that reduces the muscle stiffness. In disabled children that have very stiff muscles, the stiffness and secondary changes in the joints may cause discomfort and pain. In this study we will check if treatment with Baclofen reduces pain in disabled children with stiff muscles.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Palsy
Keywords
nursing homes, children, ages 1-18 years, spastic quadriplegia

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
group a
Arm Type
Experimental
Arm Description
Baclofen followed by Placebo
Arm Title
group b
Arm Type
Experimental
Arm Description
Placebo followed by Baclofen
Intervention Type
Drug
Intervention Name(s)
oral baclofen + placebo
Intervention Description
Group A will be given 13 weeks of oral baclofen followed by a 2-week non-treatment (washout) period, and then 13 weeks of oral placebo. For participants who with weight under 15 Kg at the time of enrolment, the initial oral baclofen dose will be 2.5 mg daily, increasing weekly over a 7-week period to 10 mg three times a day, and will be continued at that dose for the following 5 weeks. For those participants who will be over 15 Kg at the time of enrollment, the starting oral baclofen dose will be 5 mg daily, increasing over a 9-week period to 20 mg three times a day, and will be continued for the next 3 weeks at that dose. At the end of each 12-week period, the drug (either baclofen or placebo) will be tapered over 6 days. Children's carers will given information on possible side effects, and asked to contact one of the researchers if any adverse events occur.
Intervention Type
Drug
Intervention Name(s)
placebo + oral baclofen
Intervention Description
Group B will receive 13 weeks of oral placebo followed by 2-week nontreatment, and then 13 weeks of oral baclofen
Primary Outcome Measure Information:
Title
care and comport questionnaires
Time Frame
28 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cerebral palsy nursing homes children ages 1-18 years spastic quadriplegia Exclusion Criteria: active epilepsy severe truncal hypotonia
Facility Information:
Facility Name
Saare Zedek Medical Center
City
Jerusalem
Country
Israel

12. IPD Sharing Statement

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Does Oral Baclofen Improve Care and Comfort in Spastic Children in Nursing Homes?

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