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Clinical Trials/NCT03468439
NCT03468439
Completed
N/A

Short Term Effect of Ultrasound and Peripheral Nerve Stimulator Guided Femoral Nerve Block With Phenol on Outcomes in People With Traumatic Spinal Cord Injury

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital0 sites14 target enrollmentJanuary 2014

Overview

Phase
N/A
Intervention
Not specified
Conditions
Spinal Cord Injuries
Sponsor
Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
Enrollment
14
Primary Endpoint
Modified Ashworth Scale
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

A pre-post descriptive study was performed to examine the immediate effects of ultrasound (US) guided femoral nerve block with phenol (UGFNBwP) in managing lower limb spasticity of individuals with traumatic spinal cord injury (SCI).

Detailed Description

Study Design: A pre-post descriptive study was performed. Objectives: To examine the immediate effects of ultrasound (US) guided femoral nerve block with phenol (UGFNBwP) in managing lower limb spasticity of individuals with traumatic spinal cord injury (SCI). Setting: Ankara, Turkey Methods: Nineteen patients with traumatic SCI presenting with lower extremity spasticity were treated with UGFNBwP. Modified Ashworth Scale (MAS) of hip flexion and knee extension, functional independence measure (FIM) motor subscale, difficulty of catheterization (DoC), hygiene score (HS), spasm frequency (SF), sleep quality (SQ) and patient satisfaction (PS) were measured in all patients prior to treatment, at first week and second month.

Registry
clinicaltrials.gov
Start Date
January 2014
End Date
December 2016
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
Responsible Party
Principal Investigator
Principal Investigator

Yasin Demir

Principal Investigator

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • Traumatic etiology
  • Duration of spinal cord injury more than twelve months
  • Spasticity of hip flexor and/or knee extensor muscle
  • Use of any oral medications to reduce spasticity at stable doses for at least one month before first assessment
  • The patients have to accept to continue same dose until end of the last assessment
  • Medical clearance to participate

Exclusion Criteria

  • Having established contracture of the knee/hip joint
  • Aged over 65 years
  • History of surgery for knee/hip disorders
  • Non-traumatic etiology

Outcomes

Primary Outcomes

Modified Ashworth Scale

Time Frame: up to 8 weeks

Scale measures muscle tone (spasticity). (min-max:0-4).Higher values represent a worse outcome.

Secondary Outcomes

  • Functional independence measure(up to 8 weeks)

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