Motor Cortex Stimulation for Parkinson's Disease

Parkinson's Disease Clinical Trial

Official title:

Motor Cortex Stimulation for Parkinson's Disease. A Prospective Double Blind Randomized Study With Cross-over

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00637260
• Other study ID #: 820117
• Status: Completed
• Phase: N/A
• First received: March 10, 2008
• Last updated: September 1, 2015
• Start date: December 2007
• Est. completion date: June 2013

Study information

• Verified date: September 2015
• Source: Catholic University, Italy
• Contact: n/a
• Is FDA regulated: No
• Health authority: Italy: Ethics Committee
• Study type: Interventional

Clinical Trial Summary

Deep Brain Stimulation represents the golden standard for surgical treatment of Parkinson disease (PD), but it is not optimally effective for controlling every motor sign and adverse events are not so infrequent Therefore, other approaches should be considered.We identified the motor cortex as a possible candidate and therefore we propose a double-blind randomized prospective study in 20 Parkinson patients in order:

• to test the efficacy of epidural motor cortex stimulation in Parkinson disease (primary endpoint: UPDRS III at 12 months at the end of the cross-over)

• to find out optimal electrode position and optimal stimulation parameters

Description:

20 Parkinsonian patients will be enrolled. After implantation of a bilateral strip electrode (Resume, Medtronic) over the motor cortex, after setting of optimal stimulation parameters, and after implantation of a neurostimulator, Medtronic, the patient will be randomly assigned to group A (Motor cortex stimulation on) or to group B ( sham stimulation) for 6 months. Randomization will be based on the output of a program based on a random number generation function that will output a 0 or 1 with a 50% chance of having a 1.

At the 6 months visit, a cross-over is scheduled: group A will receive sham stimulation and group B will receive stimulation of the motor cortex for the next 6 months. In group A, the stimulation of the motor cortex will be resumed before the end of the 6 month sham stimulation, when the clinical status of the patient will come back to the status quo ante (UPDRS score equal to baseline pre-implant score).

Both the patients and the evaluating neurologists and neuropsychologists will be blind; only the neurosurgeon will know the state of the stimulator (on or off) and the position and parameters of MCS.

At 12 months, all the patients will be programmed as stimulation on and followed up for further 18 months. At 30 months visit, the clinical evaluation will be performed in on stim-on med, on stim-off med conditions; then the stimulator will be switched off for 1 month and the clinical evaluation will be repeated in off stim-off med and off stim-on med conditions.

The primary endpoint will be the UPDRS III at 12 months (end of the cross over), and subsequently at 18 and 30 months. We will compare the clinical results with the precise site of the stimulating electrodes and we will try to correlate the clinical results with the amount of inhibition induced by motor cortex stimulation.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 13
• Est. completion date: June 2013
• Est. primary completion date: June 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: N/A and older

Eligibility

Inclusion Criteria:

1. Idiopathic PD as diagnosed by a neurologist - a movement disorders specialist, according to the Parkinson Disease Brain Bank criteria, with asymmetrical bradykinesia, rigidity, tremor and postural instability (at least 3 from the above)

2. Significant clinical response to Levodopa (improvement of UPDRS motor score > 20%).

3. Disease duration > 5 years

4. Advanced stage of disease:

5. UPDRS motor score in off condition >/= 40/108

6. Hoehn & Yahr stage >/= 3

7. DBS surgery not indicated or expressly refused by the patient

8. Antiparkinsonian therapy stable for at least one month prior to implant

9. Capability to give informed consent to surgery and to the study.

Exclusion Criteria:

1. Severe cognitive impairment or dementia

2. Psychiatric disturbances with the exception of mild anxiety or depression and drug-induced psychiatric symptoms (i.e. benign hallucinations)

3. History of epilepsy or documented electroencephalographic abnormalities suggesting epilepsy

4. Previous neurosurgery of the brain (DBS or lesioning of the basal ganglia, fetal tissue transplantation )

5. Lack of informed consent

6. History of drug or alcohol abuse

7. Poor general conditions increasing surgical risk or severe illness with poor prognosis.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Outcomes Assessor), Primary Purpose: Supportive Care

Related Conditions & MeSH terms

• Parkinson Disease
• Parkinson's Disease

Intervention

Device:
• Motor cortex stimulation on.
The parameters of stimulation will be: contact 0 cathode, contact 3anode, 120microsec, 80 Hz, subthreshold for any movement or sensation, usually 3-5Volts. The stimulator will be switched on, continuously.
• motor cortex stimulation off
The parameters of stimulation will be: contact 0 cathode, contact 3 anode, 120microsec, 80 Hz, subthreshold for any movement or sensation, usually 3-5 volts. The stimulator will be switched off.

Locations

Country	Name	City	State
Italy	Università Cattolica - Policlinico Gemelli - Neurochirurgia Funzionale	Roma

Sponsors (2)

Lead Sponsor	Collaborator
Catholic University, Italy	Medtronic

Country where clinical trial is conducted

Italy, 

References & Publications (3)

Cioni B, Meglio M, Perotti V, De Bonis P, Montano N. Neurophysiological aspects of chronic motor cortex stimulation. Neurophysiol Clin. 2007 Dec;37(6):441-7. Epub 2007 Nov 1. Review. — View Citation

Cioni B. Motor cortex stimulation for Parkinson's disease. Acta Neurochir Suppl. 2007;97(Pt 2):233-8. Review. — View Citation

Pagni CA, Altibrandi MG, Bentivoglio A, Caruso G, Cioni B, Fiorella C, Insola A, Lavano A, Maina R, Mazzone P, Signorelli CD, Sturiale C, Valzania F, Zeme S, Zenga F. Extradural motor cortex stimulation (EMCS) for Parkinson's disease. History and first results by the study group of the Italian neurosurgical society. Acta Neurochir Suppl. 2005;93:113-9. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	UPDRS III		12 months - end of crossover	No
Secondary	UPDRS III		18, 30 and 31 months	No
Secondary	UPDRS		6,12, 18, 30, 31 months	No
Secondary	Parkinson's disease quality of life scale(PDQL)		6, 12, 18, 30, 31 months	No
Secondary	Neuropsychological and mood evaluation		6, 12, 18, 30 months	Yes
Secondary	Drug therapy		6, 12, 18, 30, 31 months	Yes