percutanous volume reduction to the intervertebral disc trough Nukleoplasty
Recruiting
- Conditions
- M51Other intervertebral disc disorders
- Registration Number
- DRKS00004958
- Lead Sponsor
- KSH, Sektion für Orthopädie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
non- sequestred lumbar intervertebral disc prolaps
Exclusion Criteria
Tumor, local or systemic infection
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method functional outcome, measures through a patient- based questionnaire, providing the oswestry disability index of the patient, filled out preoperativ and postoperativ after 2 days/ 14 days/ 2 month/ 6 month/ 1 year and 2 years.
- Secondary Outcome Measures
Name Time Method complication rate perioperative, assessed through the data provided by the surgeon and the doctoral reference until the direct dismisson of the patient from the hospital