Transcranial Temporal Interference Stimulation In Severely Brain Injured Patients With Disorders of Consciousness
Recruiting
N/A
Interventional Study
Disorders of Consciousness
Severe Brain Injury
Unresponsive Wakefulness Syndrome
Minimally Conscious State
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 65
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 10 (estimated)
- Sponsor
- Xijing Hospital · Other
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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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* traumatic and nontraumatic etiology of VS/UWS or MCS according to published diagnostic criteria.
Exclusion Criteria:
* 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…
Contacts