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NCT05626608Recruiting

Continuous Electrical Neuromodulation of the Globus Pallidus Intern in Parkinson's Disease by the Directional Electrode CARTESIA™

Neuromodulation électrique Continue du Globus Pallidus Dans la Maladie de Parkinson Par l'électrode Directionnelle CARTESIA™

Source: ClinicalTrials.gov · Last updated 28 Nov 2025

Brief summary (registry, in English)

Many patients have benefited from the implantation of brain stimulation electrodes for the treatment of various motor signs of Parkinson's disease in the phase of motor fluctuations. This technique has significantly improved the motor symptomatology of Parkinson's disease and the dyskinesias induced by pharmacological treatment. Technological advances in the field of deep brain stimulation (DBS) could improve the benefit of this therapeutic tool. therapeutic tool. While using directional electrodes, it remains possible to program the stimulation in conventional ring mode.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
10 (estimated)
First submitted
7 Nov 2022
Start date
28 Apr 2023
Primary completion date
28 Oct 2026
Lead sponsor
University Hospital, Montpellier
NCT number
NCT05626608

What you commit to

  • Study type: Interventional
  • Planned participants: 10
  • From 28 Apr 2023 to the primary completion date, 28 Oct 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Characterized depressive episode (BDI\>25) (depressive episodes prior to inclusion and completed at the time of inclusion will not be considered as a non-inclusion criterion)
  • Absolute MRI contraindications: Pacemaker or neurosensory stimulator or implantable defibrillator; Cochlear implants; Ocular or cerebral ferromagnetic foreign bodies close to nerve structures
  • Surgical contraindication

Other illness

  • Psychotic episodes (Brief Psychiatric Rating Scale, BPRS) (mild hallucinations or acute psychotic episodes preceding the screening and inclusion period and completed at the time of inclusion will not be considered as non-inclusion criteria)
  • Dementia (Mattis DRS score \<125)
  • Contraindication revealed by abnormal cerebral MRI (after-effects of stroke, vascular malformations, major cerebral atrophy)
  • Failure to obtain written informed consent after a period of reflection

Other

  • Contraindication to general anesthesia
  • Relative MRI contraindications: Metallic prostheses, especially orthodontic braces; Patient agitation; Pregnant women; Ventriculoperitoneal neurosurgical shunt valves; Tattoos containing iron particles
  • Serious intercurrent pathology
  • Pregnancy in progress or planned during the study period, Pregnant or breastfeeding women or women in a state of procreation without contraception Women who are pregnant or breastfeeding or in a state of procreation without effective contraception
  • Impossibility or refusal of regular follow-up of at least 30 months
  • Participation in other interventional research
  • Adult protected by law or patient under guardianship or curatorship
  • Patient unable to use the remote control and charging system properly or who does not have a person who can assist them in this process
  • Not being affiliated to a French social security system or being a beneficiary of such a system

Who the study is looking for

  • A diagnosis of bilateral idiopathic Parkinson's disease according to the British Brain Bank criteria (bradykinesia and rigidity or resting tremor)
  • Parkinson's disease that has been evolving for several years (\>4 years)
  • Persistence of a good sensitivity to L-Dopa, essential criterion in the selection, except for tremor (Improvement in Parkinson's disease symptoms of at least 30% measured on the UPDRS, section III)
  • A UPDRS (Unified Parkinson Disease Rating Scale) part III motor score \>25 under MEDOFF conditions
  • Patient with tremor not controlled́ by treatment and which represents the bulk of the symptomatology. Patient will require stable treatment throughout the study.
  • Patient with major motor fluctuations with prolonged blocking and/or dyskinesias
  • Be a candidate for PCS and bilateral electrode implantation in the STN.
  • A Hoehn and Yahr scale score ≤ 2.5 under best MED-ON conditions
  • A UPDRS section II activities of daily living score \> 6
  • Patient without comorbidities that do not allow the patient to undergo general anesthesia general anesthesia or a neurosurgical procedure or interfering with the follow-up required by the protocol

Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Centre Hospitalier Uniersitaire de Montpellier
Coordinator of this site? Confirm its status
MontpellierFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.