MedTrace Logo

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

NCT06851156 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2025-04-09

No results posted yet for this study

Summary

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.

Conditions

  • Disorders of Consciousness
  • Severe Brain Injury
  • Unresponsive Wakefulness Syndrome
  • Minimally Conscious State

Interventions

DEVICE

tTIS

CM-pf tTIS

Sponsors & Collaborators

  • Xijing Hospital

    lead OTHER

Principal Investigators

  • wen Jiang, phD · Xijing Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-04-07
Primary Completion
2025-12-31
Completion
2025-12-31

Countries

  • China

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06851156 on ClinicalTrials.gov