Cervical radicular pain: A randomised controlled trial comparing percutaneous plasma discectomy and anterior cervical discectomy.
- Conditions
- cervical radicular pain1002837710041543
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 94
Radicular pain of the lower cervical spine (C4-7) with complaints of radicular pain (VAS (0-100) as a result of a contained soft disc hernia with or without neck pain, without improvement in at least 8 weeks of conservative therapy.
Age below 18 and above 65 years; Pregnancy; Anticoagulant drug therapy and/or disturbed coagulation; Infections/ tumours; Previous spinal surgery in cervical region; Extruded disc fragment; bony spurs; calcified disc; Herniation > 5 mm; Disc: maximal 50% loss of height; Neurodegenerative diseases, including lesions of the spinal cord; Lack of cooperation of the patient; Patients who are not able to complete the questionnaires, according to the referring doctor; Drugs/medication/ alcohol addiction; Serious psychopathology;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The influence of treatment on the intensity of pain, the global perceived<br /><br>effect.</p><br>
- Secondary Outcome Measures
Name Time Method <p>The functional status and the health-related quality of life and<br /><br>cost-effectiveness</p><br>