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Intermittent Theta Burst Stimulation and Repetitive Transcranial Magnetic Stimulation Combined With Robotic Rehabilitation on Ambulation in Spinal Cord Injury Patients - Trial NCT06248476

Access comprehensive clinical trial information for NCT06248476 through Pure Global AI's free database. This phase not specified trial is sponsored by Gaziler Physical Medicine and Rehabilitation Education and Research Hospital and is currently Recruiting. The study focuses on Spinal Cord Injuries. Target enrollment is 30 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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Trial Details
ClinicalTrials.gov โ€ข NCT06248476
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Intermittent Theta Burst Stimulation and Repetitive Transcranial Magnetic Stimulation Combined With Robotic Rehabilitation on Ambulation in Spinal Cord Injury Patients
Effect of Intermittent Theta Burst Stimulation and Repetitive Transcranial Magnetic Stimulation Combined With Robotic Rehabilitation on Ambulation and Lower Extremity Motor Function in Chronic Spinal Cord Injury Patients

Study Focus

Spinal Cord Injuries

Transcranial Magnetic Stimulation

Interventional

device

Sponsor & Location

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

Ankara, Turkey

Timeline & Enrollment

N/A

Mar 01, 2023

Jul 01, 2024

30 participants

Primary Outcome

Lower extremity motor score

Summary

Comparison of different types of transcranial magnetic stimulation techniques which are
 intermittent theta burst stimulation (iTBS) and high frequency repetitive transcranial
 magnetic stimulation (rTMS) in patients with spinal cord injury

ICD-10 Classifications

Sequelae of injury of spinal cord
Other and unspecified injuries of thoracic spinal cord
Other and unspecified injuries of cervical spinal cord
Other injury of lumbar spinal cord
Injury of spinal cord, level unspecified

Data Source

ClinicalTrials.gov

NCT06248476

Device Trial