Lateral Cord Stimulation as a New Treatment for Refractory Spastic Cerebral Palsy (Andreani1)
Primary Purpose
Cerebral Palsy, Spasticity
Status
Not yet recruiting
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Lateral spinal cord surgical implant of electrodes
Sponsored by
About this trial
This is an interventional treatment trial for Cerebral Palsy focused on measuring Dysarthria, Electrical Stimulation, Lateral Cord Stimulation, Spasticity, Treatment
Eligibility Criteria
Inclusion Criteria:
- Aged sixteen or older
- Spastic Cerebral Palsy with stable condition
- Motor disability unilateral or predominantly unilateral.
- Troubles of speech clinically evident.
- Normal or Slightly sub-normal I.Q
- No psychiatric disorders.
Exclusion Criteria:
- Severe cardiac or respiratory troubles
- Fixed abnormal postures (except if previously corrected by orthopedic surgery)
- Chronic recurrent bronchial or pulmonary infections
- Chronic recurrent urinary infections
- Severe osteoporosis on affected limbs
- Chronic skin ulcerations.
Sites / Locations
- Provincial Program of Neuromodulation
- Klinikummagdeburg
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Spasticity, Cerebral Palsy
Arm Description
To perform a Lateral spinal cord surgical implant of electrodes for electrical neuromodulation of a cohort of selectyed patients with refractory Spastic Cerebral Palsy To compare spasticity and speech trouble´s evolution on a cohort of treated patients, by evaluating their pre and post operative status into one year follow up.
Outcomes
Primary Outcome Measures
Ashworth Scale
The Ashworth scale has 5 points, they are: 1) no increase in muscle tone; 2) slight increase giving a catch when part is moved in flexion or extension; 3) more marked increase in tone but only after part is easily flexed; 4) considerable increase in tone; and 5) passive movement is difficult and affected part is rigid in flexion or extension
Secondary Outcome Measures
Barthel Index
The Barthel Index consists of 10 items that measure a person's daily functioning specifically the activities of daily living and mobility of the patient. The items include feeding, moving from wheelchair,etc, and the whole evaluation is from 100 maximum what means total independence, to 0, absolute dependence
Full Information
NCT ID
NCT02199015
First Posted
July 17, 2014
Last Updated
October 27, 2022
Sponsor
Juan Carlos M. Andreani MD
Collaborators
Fundación CENIT
1. Study Identification
Unique Protocol Identification Number
NCT02199015
Brief Title
Lateral Cord Stimulation as a New Treatment for Refractory Spastic Cerebral Palsy
Acronym
Andreani1
Official Title
Lateral Cord Electrical Stimulation Can Improve Spasticity in Chronic Spastic Cerebral Palsy
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
June 1, 2024 (Anticipated)
Primary Completion Date
April 1, 2026 (Anticipated)
Study Completion Date
December 31, 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Juan Carlos M. Andreani MD
Collaborators
Fundación CENIT
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The aim of our work is to investigate whether electrical Lateral Cord Stimulation (LCS) causes an inhibitory and modulatory action by indirect cerebellar activation, so releasing spasticity and the spastic syndrome in selected cases of patients with cerebral palsy
Detailed Description
PROJECT Lateral Cord Stimulation was thought by the author to be employed in patients with spastic cerebral palsy with the aim to improve tonus, motor function and speech.
Nevertheless, as it has been demonstrated as acting on the basic phenomena related with spasticity, it's to say the propagated spinal responses, its use could be extended to other forms of spastic disease, like spastic limbs post stroke, brain congenital malformations producing spasticity and motor disorders as the main signs, post anoxic encephalopathy, etc.
In this preliminary clinical trial, classed as phase 3, our sample must be very limited to assure stable conditions for statistical significance, hence our group is going to be circumscribed to certain conditions and pathology.
In the future, as long the method could spread its use, the extension on indications in other pathological conditions is advisable thus, its possibilities of marketing could be enlarged with its use in a broader spectrum of spastic patients.
Calculated risks are similar to those related with the ancient surgical technique called "Scoville"technique, currently employed time ago for cervical discectomy (6) Investigational plan The purpose of this clinical trial is to release spasticity and by this means improve the condition of patients with spastic cerebral palsy by extradural lateral cord electrical stimulation, by using currently employed electrodes and neurostimulators Those devices are already FDA approved and currently used for Dorsal Column Stimulation with the objective to treat chronic Pain and spasticity (Spasmodic Torticollis).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Palsy, Spasticity
Keywords
Dysarthria, Electrical Stimulation, Lateral Cord Stimulation, Spasticity, Treatment
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Spasticity, Cerebral Palsy
Arm Type
Experimental
Arm Description
To perform a Lateral spinal cord surgical implant of electrodes for electrical neuromodulation of a cohort of selectyed patients with refractory Spastic Cerebral Palsy To compare spasticity and speech trouble´s evolution on a cohort of treated patients, by evaluating their pre and post operative status into one year follow up.
Intervention Type
Device
Intervention Name(s)
Lateral spinal cord surgical implant of electrodes
Other Intervention Name(s)
Implant of Neurostimulators (electrical generators)
Intervention Description
The procedure is based on the classic approaches to posterior cervical region for herniated discs, actually not longer employed for that aim A unilateral hemilaminectomy will be performed at C3-C4 level, starting from 4th cervical spinous process.
A multicontact electrode will be placed on the lateral surface of the spinal cord that will be subcutaneusly connected to an implanted pulse generator (IPG).
Primary Outcome Measure Information:
Title
Ashworth Scale
Description
The Ashworth scale has 5 points, they are: 1) no increase in muscle tone; 2) slight increase giving a catch when part is moved in flexion or extension; 3) more marked increase in tone but only after part is easily flexed; 4) considerable increase in tone; and 5) passive movement is difficult and affected part is rigid in flexion or extension
Time Frame
Day 0 baseline evaluation. One post operative evaluation every 30 day during six months
Secondary Outcome Measure Information:
Title
Barthel Index
Description
The Barthel Index consists of 10 items that measure a person's daily functioning specifically the activities of daily living and mobility of the patient. The items include feeding, moving from wheelchair,etc, and the whole evaluation is from 100 maximum what means total independence, to 0, absolute dependence
Time Frame
Day 0 baseline evaluation. One post operative evaluation every 30 day during six months
Other Pre-specified Outcome Measures:
Title
Functional Independence Measure (FIM)- for speech
Description
It is global independence assessment. In this case, we are going to take only those related to speech for disartria´s evaluation
Time Frame
Day 0 baseline evaluation. One post operative evaluation every 30 day during six months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Aged sixteen or older
Spastic Cerebral Palsy with stable condition
Motor disability unilateral or predominantly unilateral.
Troubles of speech clinically evident.
Normal or Slightly sub-normal I.Q
No psychiatric disorders.
Exclusion Criteria:
Severe cardiac or respiratory troubles
Fixed abnormal postures (except if previously corrected by orthopedic surgery)
Chronic recurrent bronchial or pulmonary infections
Chronic recurrent urinary infections
Severe osteoporosis on affected limbs
Chronic skin ulcerations.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Juan Carlos Andreani, MD
Phone
5491150531392
Email
jcmandreani@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juan Carlos Andreani, MD
Organizational Affiliation
Sociedad Argentina de Neuromodulación
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Werner Braunsdorf, MD
Organizational Affiliation
Klinik von Magdeburg - Germany
Official's Role
Principal Investigator
Facility Information:
Facility Name
Provincial Program of Neuromodulation
City
La Plata
State/Province
Buenos Aires
ZIP/Postal Code
1045
Country
Argentina
Facility Name
Klinikummagdeburg
City
Magdeburg
ZIP/Postal Code
399130
Country
Germany
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Yes, we plan to share data as long as participants are recruited. Because there are not yet patients, we do not have data to share
Citations:
PubMed Identifier
22151096
Citation
Andreani JC, Guma C. New animal model to mimic spastic cerebral palsy: the brain-damaged pig preparation. Neuromodulation. 2008 Jul;11(3):196-201. doi: 10.1111/j.1525-1403.2008.00166.x.
Results Reference
background
PubMed Identifier
22151097
Citation
Andreani JC, Guma C. Lateral cord stimulation decreases spastic electromyographic spreading: responses in a brain-damaged pig preparation. Neuromodulation. 2008 Jul;11(3):202-7. doi: 10.1111/j.1525-1403.2008.00167.x.
Results Reference
background
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Lateral Cord Stimulation as a New Treatment for Refractory Spastic Cerebral Palsy
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