NCT07477613Toboroz
Implantable Brain-Computer Interface for Upper-Limb Recovery After Stroke
Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. júl. 7.
Rövid összefoglaló (regiszter, angolul)
The clinical investigation will take place in three phases: * A pre-selection/selection phase to ensure that the patient (lesion, symptoms, ability of our tools to detect your movement intentions, etc.) is suitable for a six-month intensive rehabilitation program using Brain-Machine Interface. * A second phase, consisting of implementing the intensive rehabilitation program, first in the traditional manner, without the Brain-Machine Interface (2 to 5 weeks), then, after implantation, with the Brain-Machine Interface (6 months). * During the third phase, only follow-up visits will be scheduled to ensure the longevity of the implants and the maintenance of the motor progress achieved through rehabilitation.
- Állapot (regiszter)
- Toboroz
- Vizsgálattípus
- Beavatkozással járó
- Résztvevők száma
- 10 (tervezett)
- Első benyújtás
- 2026. febr. 24.
- Kezdés
- 2026. ápr. 8.
- Elsődleges befejezés
- 2029. ápr. 8.
- Fő szponzor
- University Hospital, Grenoble
- Betegségek
- Stroke (szélütés)
- NCT-szám
- NCT07477613
Mit vállalsz
- Vizsgálat típusa: Beavatkozással járó
- Tervezett résztvevők: 10
- 2026. ápr. 8. és az elsődleges befejezés (2029. ápr. 8.) között
- 1 helyszín, 1 országban
- Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket
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Korábbi kezelés
- Contraindication for general anesthesia and for the surgery (such as thrombocytopenia, …)
- Previous stroke (symptomatic deficit)
- Presence of brain implants of metal clips and/or brain stimulators
- Contraindication for general anesthesia and for the surgery (such as thrombocytopenia, …)
- Previous stroke (symptomatic deficit)
- Presence of brain implants of metal clips and/or brain stimulators
- Shape of the skull in the implantation site not concordant with the WIMAGINE implant, assessed by anatomical MRI
Más betegség
- Pre-existing dementia or significant cognitive deficits (MoCA)
- Lesions on the scalp area, skin infections or dermatitis
- A health status, any clinical condition (eg, short life expectancy, and coexisting disease) or other characteristic that precludes appropriate diagnosis, treatment, or follow-up in the trial
- Pre-existing dementia or significant cognitive deficits (MoCA)
- Lesions on the scalp area, skin infections or dermatitis
- A health status, any clinical condition (eg, short life expectancy, and coexisting disease) or other characteristic that precludes appropriate diagnosis, treatment, or follow-up in the trial
- Persons referred to in Articles L1121-5 to L1121-7 of the French Public Health Code (CSP), corresponding to all protected persons: pregnant women, women in labor, breastfeeding mothers, individuals deprived of liberty by judicial or administrative decision, individuals undergoing psychiatric care under Articles L.3212-1 and L.3213-1 who are not covered by Article L.1121-8, individuals admitted to a healthcare or social institution for purposes other than research, and minors.
- Moreover, patient will not be included for implantation (exclusion criteria), if he is not eligible for a BCI rehabilitation protocol, as determined by the clinical team after multimodal selection tests. As examples, it can be due to:
Egyéb
- Contraindication for Magnetic Resonance Imaging (MRI), Computed Tomography (CT-scan), Positron Emission Tomography (PET-scan)
- Contraindication for Transcranial Magnetic Stimulation (TMS), Electroencephalography (EEG), Magnetoencephalography (MEG)
- Severe leukoaraiosis
- Intolerance to electrical stimulation
- Major spasticity in the upper limb (4 or 5 in the scale of Modified Ashworth Scale - MAS)
- Epileptiform focus, even without clinical repercussions
- Severe dystonia/involuntary movements
- Patients with any of the following criteria cannot be included in this investigation:
- Contraindication for MRI, CT-scan, PET-scan
- Contraindication for TMS, EEG, MEG
- Severe leukoaraiosis
- Intolerance to electrical stimulation
- Major spasticity in the upper limb (4 or 5 in the scale of Modified Ashworth Scale - MAS)
- Epileptiform focus, even without clinical repercussions
- Severe dystonia/involuntary movements
- No existing residual corticospinal tracts proven tractography and/or Motor Evoked Potential (MEP)
- Unability to control a BCI or unwillingness to follow a BCI rehabilitation program, assessed by MEG-BCI
- Unability to activate any residual motor regions during motor imagery assessed by EEG and functional MRI (fMRI)
Kiket keres a vizsgálat
- Male or female, 18-70 years-old included
- Hemispheric ischemic stroke (> 1.5 cm on 2 imaging slices): cortical and/or subcortical lesion
- No decompressive craniectomy procedure performed
- Single unilateral stroke occurred 6 months to 18 months ago
- Disabling motor deficit of upper limb
- Patient able to follow a rehabilitation program
- Written consent to participate in the study from the patient and his/her legal representative
- Person affiliated to the social security system or beneficiary of such a system
- Highly effective or at least acceptable birth control method for women of childbearing potential
Életkor a regiszterben: 18 év – 70 év · Nem: nők és férfiak · Egészséges önkénteseket nem fogad
Helyszínek (1)
Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.
| Helyszín | Város | Ország | Helyszín állapota |
|---|---|---|---|
| CHUGA | Grenoble | Franciaország | Toboroz |
Ez az oldal tájékoztatás, nem orvosi tanács. Bármely vizsgálatról az orvosoddal beszélj.