Motor and Premotor Cortex Stimulation for Treatment of Secondary Focal Dystonia With Striato Palliadal Lesion : Evaluation of Safety and Effectiveness

NCT ID: NCT00505323

Last Updated: 2014-07-08

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 5 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-09-30
• Study Completion Date: 2011-06-30

Brief Summary

Dystonia is a neurological movement disorder in which sustained muscle contractions cause twisting and repetitive movements or abnormal postures. This disease is very heterogeneous and can have many causes. Current treatments (drugs, pallidal stimulation) improve primary generalized dystonias; however they are ineffective for focal dystonias following brain damage.

Cortex stimulation is a present and effective technique used in the treatment of chronic pain and could represent an interesting strategy to treat focal dystonias. This is the aim of the present study.

Detailed Description

Pilot study included 6 centres (Clermont-Ferrand, Bordeaux, Paris, Créteil, Lyon and Grenoble)

Study progress :

• 3 months to 1 month before chirurgical intervention : selection of patient that could be included in the protocol.
• 15 days to 8 days before chirurgical intervention : inclusion visit.
• Operating phase : under anaesthesia, implantation of the neurostimulator and its components, and adjustment of stimulation parameters.
• 1 month after chirurgical intervention : checking that all is fine (detection of undesirable events)
• 2 months to 5 months after chirurgical intervention: randomization (double blind): the stimulator is put on position On or OFF
• 5 months after chirurgical intervention : Stimulators of all patients are stopped for one month whatever the group they belong.
• 6 months to 9 months after chirurgical intervention: Stimulatiors are put on position On or OFF (cross over with the first period).
• 9 months to 13 months after chirurgical intervention: Stimulators of all patients are started for four months whatever the group they belong.
• 13 months after chirurgical intervention : study end

Conditions

Focal Dystonia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Interventions

Implantation of neurostimulators and their auxiliary components

Implantation neurostimulators and their auxiliary components :

Stimulateur KINETRA TM modèle 7428, Electrode Resume II modèle 3587A, Extension kit DBS 7482

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Age : >18 years and < 65 years
• Evolution time of dystonia > 1 year
• Clinical stability of dystonia = 1 year
• Secondary dystonia due to a focal lesion (vascular or anoxic) of central grey nuclei
• Inefficiency of others treatments (anticholinergic, benzodiazepine, neuroleptique, botulinum toxin, etc.)
• Stability of treatment >3 months
• Agreement of patients
• Affiliation to social security

Exclusion Criteria

• Significant heart vascular disease; significant respiratory, metabolic, renal or hepatic diseases
• Significant clinical and biological anomalies
• Disease or treatment in favour in bleeding
• Sever cognitive disorders
• Psychiatric evolutionary pathology
• Counter-indication during inclusion examination
• Chirurgical counter-indication
• Pregnant women ou women who nurse
• Person who participate to an other study

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Medtronic

INDUSTRY

Sponsor Role: collaborator

University Hospital, Clermont-Ferrand

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Franck DURIF, Pr

Role: PRINCIPAL_INVESTIGATOR

Other Identifiers

PHRC N 2007 DURIF

Identifier Type: -

Identifier Source: secondary_id

2007-A00100-53

Identifier Type: -

Identifier Source: org_study_id