Transcranial Temporal Interference Stimulation In Severely Brain Injured Patients With Disorders of Consciousness

ConditionsDisorders of Consciousness Severe Brain Injury Unresponsive Wakefulness Syndrome Minimally Conscious State

Trial statusRecruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age18-65

SponsorXijing Hospital

About this trial

The purpose of this academic lead study is to explore the effect of noninvasive neuromodulation of the CM-pf via tTIS for patients with disorders of consciousness.

Eligibility criteria

Qualifiers

traumatic and nontraumatic etiology of VS/UWS or MCS according to published diagnostic criteria.

Disqualifiers

patients in coma, with less than 1 week after acute brain insult, with fluctuating diagnosis on baseline assessment, and with a metallic cerebral implant or pacemaker, and with epilepsy.

Trial design

Treatments tested in this trial

tTIS

Treatment groups

10 Participants

are divided into 1 treatment group

Sponsors and collaborators

Xijing Hospital

Lead sponsor

Source ClinicalTrials.gov