Skip to main content
Clinical Trials/NCT05466110
NCT05466110
Recruiting
Not Applicable

sPinal coRd stimulatiOn coMpared With Lumbar InStrumEntation for Low Back Pain After Previous Lumbar Decompression (PROMISE): a Prospective Randomized Controlled Study

University Hospital Augsburg1 site in 1 country84 target enrollmentMarch 20, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Failed Back Surgery Syndrome
Sponsor
University Hospital Augsburg
Enrollment
84
Locations
1
Primary Endpoint
Oswestry disability index / ODI
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

Low back pain affects people of all ages and has become the leading cause of living with disability worldwide. Patients, suffering from persistent pain after spinal surgery in the absence of any clear spinal pathology are defined of having a "failed back surgery syndrome (FBSS)" and treatment of FBSS remains a great controversy in the spinal community. Apart from conservative treatment, spinal fusion remains as therapeutic option. Furthermore, minimal invasive Neuromodulation techniques might be a promising alternative. Aim of this randomized interventional multi center study is to compare treatment success in FBSS patients with either spinal cord stimulation (SCS) or fusion surgery, 12 months after intervention according to the Oswestry Disability Index (ODI) and other scales and scores. Radiological and health economic outcome also will be analysed for thorough comparison of techniques. Additionally, the safety of the interventions needs to be compared.

Registry
clinicaltrials.gov
Start Date
March 20, 2023
End Date
May 2025
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital Augsburg
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age ≥18 years
  • Symptomatic degenerative disc disease with LBP as a predominant symptom for at least 6 months following pervious surgery for disc herniation
  • ODI score at least 21
  • Correctly signed informed consent form

Exclusion Criteria

  • Spinal stenosis resulting in spinal claudication or neurological deficits
  • Spinal Instability (\> 3 mm Motion on dynamic Lumbar X-rays)
  • Major psychiatric disorder

Outcomes

Primary Outcomes

Oswestry disability index / ODI

Time Frame: 12 months after intervention

A patient reported outcome measure to rate pain and disability

Secondary Outcomes

  • Pain medication(12 months after intervention)
  • hospital length of stay(through study completion, an average of 2 years)
  • Adverse events(12 months after intervention)
  • SF36(12 months after intervention)
  • EuroQOL 5D(12 months after intervention)
  • Crossover rates(12 months after intervention)

Study Sites (1)

Loading locations...

Similar Trials