Actively Recruiting

Phase 1
Age: 18Years - 70Years
All Genders
NCT04969042

Closed-loop Functional Spinal Cord Stimulation in Patients With Spinal Cord Injury

Led by Luming Li · Updated on 2021-07-20

10

Participants Needed

1

Research Sites

313 weeks

Total Duration

On this page

Sponsors

L

Luming Li

Lead Sponsor

B

Beijing Tsinghua Changgeng Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this experiment is to evaluate the efficacy of Closed-loop Functional Spinal Cord Stimulation on Walking Rehabilitation in Patients after Spinal Cord Injury

CONDITIONS

Official Title

Closed-loop Functional Spinal Cord Stimulation in Patients With Spinal Cord Injury

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18~70
  • Spinal cord injury staging (AIS) A, B, C, or D
  • Level of lesion is T10 and above
  • Distance between lesion and conus >60mm
  • Injured time more than 3 months
  • Capable of participating in rehabilitation program
  • Agree to comply with all study conditions and attend all required training and visits
Not Eligible

You will not qualify if you...

  • Obvious psychiatric disorder preventing completion of questionnaires
  • Cognitive impairment
  • Severe autonomic reflex disorder
  • Severe muscle atrophy and joint contracture
  • Unable to participate in spinal cord stimulation surgery or follow-up visits
  • Life expectancy less than 12 months
  • Abnormal blood or physiological exams preventing surgery, such as coagulation disorders or kidney/liver abnormalities
  • Uncontrollable hypertension, heart diseases, respiratory diseases, or use of related medicine in last 3 months
  • Unsuitable candidates from principal investigator's perspective

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

National Engineering Laboratory for Neuromodulation

Beijing, Beijing Municipality, China

Actively Recruiting

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Research Team

Y

Yang Lu, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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