A MULTI-CENTER, POST MARKETING SURVEILLANCE STUDYTO MONITOR THE SAFETY AND PERFORMANCEOF THE BARRICAID® ARD IN THE TREATMENT OF BACK ANDRADICULAR PAIN CAUSED BY PRIMARY LUMBAR DISCHERNIATIO
- Conditions
- hernia10009720lumbal disc herniation
- Registration Number
- NL-OMON32568
- Lead Sponsor
- Canisius Wilhelmina Ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 30
Any subject meeting all of the following criteria will be considered acceptable for inclusion in this trial.1. Age 18 to 75 years old (male or female).2. Patients with posterior or posterolateral disc herniations at one or two levels between L1 andS1 with radiographic confirmation of neural compression using CT and/or MRI.3. At least six (6) weeks of failed, conservative treatment prior to surgery, including physicaltherapy, use of anti-inflammatory medications at maximum specified dosage and/oradministration of epidural/facet injections.;4. Minimum posterior disc height of 3mm at the index level(s).5. Lower back pain and/or sciatica with or without spinal claudication.6. Oswestry Questionnaire score of at least 40/100 at baseline.7. VAS leg pain of at least 40/100 at baseline.8. Psychosocially, mentally and physically able to fully comply with the clinical protocol and willingto adhere to follow-up schedule and requirements.
3.1.2 EXCLUSION CRITERIAAny subject meeting any one of the following criteria will be excluded from enrollment into the trial:1. Spondylolisthesis Grade II or higher2. Subject requires uni or bilateral facetectomy to treat leg/back pain3. Subject has back or non-radicular leg pain of unknown etiology.4. Prior fusion (with or without instrumentation), motion preservation, facetectomy or IDETsurgery at the index lumbar vertebral level5. Subject*s requiring a spine DEXA (i.e., patients with SCORE of = 6) with a T Score lessthan -2.0 at the index level.6. Subject has clinically compromised vertebral bodies at the index level(s) due to any traumatic,neoplastic, metabolic, or infectious pathology.7. Subject has sustained pathologic fractures of the vertebra or multiple fractures of the vertebraor hip.8. Subject has scoliosis of greater than ten (10) degrees (both angular and rotational).9. Any metabolic disease bone disease that has not been stabilized for at least three months
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>NVT</p><br>
- Secondary Outcome Measures
Name Time Method <p>NVT</p><br>