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Clinical Trials/NCT02663310
NCT02663310
Unknown
Not Applicable

Surgical Decompression/Untethering Combined With Weight Bearing Rehabilitation in Chronic Spinal Cord Injury Subjects

Kunming Tongren Hospital1 site in 1 country30 target enrollmentJuly 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Spinal Cord Injuries
Sponsor
Kunming Tongren Hospital
Enrollment
30
Locations
1
Primary Endpoint
Change of Kunming Locomotor Scale in 1 year
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to investigate the efficacy of surgical decompression/untethering, combined with weight bearing rehabilitation, on neurological recovery following chronic spinal cord injury.

Detailed Description

Safety Issues: Safety issues need to be watched are: occurrence of known and unknown undesirable incidences, moving up injury levels, loss of previously preserved neurological functions, vital physical signs, and worsening of EKG and lab results. If unforeseen issues occur, patients will be consulted to determine whether treatments will be continued. Adverse events: Adverse events may occur during the trail and these events will be recorded. The severity of the events and their relationship to the experimental therapy will be determined, documented and reported to the Data Monitoring and Safety Committee who will determine how these events will be handled if they occur.

Registry
clinicaltrials.gov
Start Date
July 2015
End Date
June 2018
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hui Zhu

Director

Kunming Tongren Hospital

Eligibility Criteria

Inclusion Criteria

  • Male or female adult subjects, 18-60 years of age
  • Have a clinical diagnosis of chronic spinal cord injury (≥ 12 months after traumatic spinal cord injury).
  • Neurological examination: ASIA-A
  • Injury levels: T1-T12 spinal levels
  • The diagnosis of spinal cord injury is confirmed by MRI
  • Subjects must be able to read, write and complete visual analogue scale
  • Voluntarily signs and dates an informed Consent form, approved by an Institutional Review Board (IRB)/Independent Ethics Committee (IEC), prior to any study-specific procedures. If a subject consents to participation but is not in a position to personally sign and date the informed consent form because of his or her physical condition, the consent must be confirmed at the time of consent orally, signed on behalf by the subject's relative, and by an impartial witness who is present throughout the whole informed consent process.

Exclusion Criteria

  • Severe head injury
  • Subjects with severe osteoporosis or joint diseases
  • Subjects with severe pressure sore
  • Sign of kidney, cardiovascular, liver disorders
  • Subjects with internal medical and/or infectious diseases (including but not limited to Hepatitis B and HIV carriers)
  • Pregnant women or women at lactation stages
  • Medically or mentally unstable according to the judgment of the investigator
  • History of multiple sclerosis or peripheral demyelination
  • Any criteria which, in the opinion of the investigator, suggests that the subject would not be compliant with the study protocol

Outcomes

Primary Outcomes

Change of Kunming Locomotor Scale in 1 year

Time Frame: Day 0, Day 15, Month 1, Month 2, Month 3, Month 4, Month 5, Month 6, and 1 year

Kunming Locomotor Scale is a 10-grade Roman numeral locomotion scoring system. Grade I, the patient can not stand; grade II, the patient was able to stand with weight support and help in fixing the knee; grade III, the patient was able to stand with weight support; grade IV, the patient was able to walk with wheeled weight support and help in fixing the knee of the weight bearing leg; grade V, the patient was able to walk with wheeled weight support; grade VI, the patient was able to walk with the help of a light four-leg support; grade VII, the patient was able to walk with a pair of crutches; grade VIII, the patient was able to walk with a cane; grade IX, the patient was able to walk without support but staggeringly; and grade X, the patient was able to walk stably without support.

Secondary Outcomes

  • Change of Numerical Rating Scale in 1 year(Day 0, Day 15, Month 1, Month 2, Month 3, Month 4, Month 5, Month 6, and 1 year)
  • Change of Modified Ashworth Scale in 1 year(Day 0, Day 15, Month 1, Month 2, Month 3, Month 4, Month 5, Month 6, and 1 year)
  • Change of Walking Index for Spinal Cord Injury in 1 year(Day 0, Day 15, Month 1, Month 2, Month 3, Month 4, Month 5, Month 6, and 1 year)
  • Change of Spinal Cord Independence Measure in 1 year(Day 0, Day 15, Month 1, Month 2, Month 3, Month 4, Month 5, Month 6, and 1 year)
  • Change of American Spinal Injury Association Impairment Scale in 1 year(Day 0, Day 15, Month 1, Month 2, Month 3, Month 4, Month 5, Month 6, and 1 year)

Study Sites (1)

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