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