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Short-term Cervical Spinal Cord Stimulation in Patients With Disorders of Consciousness After Intracerebral Hemorrhage

The Safety and Efficacy of Short-term Cervical Spinal Cord Stimulation in Patients With Disorders of Consciousness After Intracerebral Hemorrhage: a Multicenter, Prospective, Randomized, Outcome-blind Interventional Study

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05922644
Acronym
SCS-ICH
Enrollment
344
Registered
2023-06-28
Start date
2023-07-01
Completion date
2030-09-01
Last updated
2023-07-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coma, Stroke

Brief summary

Disorders of consciousness (DOC) refers to the persistent loss of consciousness after 28 days in patients with brain injury caused by trauma, stroke, or hypoxia. It includes coma, vegetative state, and minimally conscious state. At present, there is no effective treatment for DOC. Only one RCT study of amantadine has proved that it may be effective for the treatment of DOC. In recent years, more evidence has shown that neuromodulation technology is beneficial to the recovery of DOC. Cervical spinal cord stimulation surgery is a new treatment method for patients with DOC. Electrodes are implanted in the high cervical spinal cord C2-C5. By adjusting different electrical stimulation parameters, it has a wake-promoting effect. In this study, patients were selected into the spinal cord stimulation group and the conventional treatment group according to the wishes of their families. The patients in the spinal cord stimulation group were given 21 days of cervical spinal cord stimulation treatment on the basis of conventional brain rehabilitation. Patients were followed up routinely and completed designated examinations at 12 months to determine the safety and efficacy of cervical spinal cord stimulation therapy.

Interventions

DEVICESCS

21 days of cervical spinal cord electrical stimulation treatment in addition to routine brain resuscitation and rehabilitation awakening treatment.

OTHERConventional

Routine brain resuscitation and rehabilitation awakening treatment.

Sponsors

Rehabilitation Hospital Affiliated to National Research Center for Rehabilitation Technical Aids
CollaboratorUNKNOWN
Shenzhen Qianhai Shekou Free Trade Zone Hospital
CollaboratorUNKNOWN
Beijing Tiantan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Age between 18 and 65 years old * Patients with postoperative consciousness disorders after cerebral hemorrhage for more than 28 days * CRS-R score meets the MCS diagnosis * Signed informed consent.

Exclusion criteria

* Secondary brain injury caused by arteriovenous malformation, cerebral aneurysm, cavernous hemangioma, brain tumor and carbon monoxide poisoning * History of previous epileptic seizures * Critical condition, unstable intracranial condition, risk of rebleeding * Unstable vital signs requiring mechanical ventilation * Contraindications for spinal cord surgery * Severe sympathetic overactivity syndrome.

Design outcomes

Primary

MeasureTime frameDescription
Change in consciousness 12 months after surgery assessed by CRS-R12 monthsThe primary efficacy indicator is change in consciousness recovery 12 months after cervical spinal cord electrical stimulation (assessed by the Coma Recovery Scale - Revised (CRS-R), ranges from 0 to 25, with higher scores mean a better outcome).

Secondary

MeasureTime frameDescription
Consciousness recovery 12 months after surgery assessed by GOS-E12 monthsThe secondary efficacy indicator is consciousness recovery 12 months after surgery (assessed by the Glasgow Outcome Scale - Extended (GOS-E) to evaluate the patient's consciousness status, ranges from 0 to 8, with higher scores mean a better outcome).

Other

MeasureTime frameDescription
Glasgow Coma Scale (GCS)12 monthsExploratory Indicators, ranges from 0 to 15, with higher scores mean a better outcome.
National Institute of Health stroke scale (NIHSS)12 monthsExploratory Indicators, ranges from 0 to 42, with higher scores mean a worse outcome.
Full Outline of UnResponsiveness (FOUR) Score12 monthsExploratory Indicators, ranges from 0 to 16, with higher scores mean a better outcome.
Disability rating scale (DRS)12 monthsExploratory Indicators, ranges from 0 to 29, with higher scores mean a worse outcome.

Countries

China

Contacts

Primary ContactYong Cao, MD
caoyong@bjtth.org+8613601362306
Backup ContactQiheng He, MD
heqiheng96@mail.ccmu.edu.cn+8615699952258

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026