Measuring cervical epidural pressure in biportal endoscopic spinal surgery
Not Applicable
Recruiting
- Conditions
- Diseases of the musculo-skeletal system and connective tissue
- Registration Number
- KCT0004075
- Lead Sponsor
- Korea University Anam Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
1) Lumbar spinal stenosis and disc herniation patients
2) Patients needing surgery who did not response to conservative treatment
3) Patients who are planned for biportal endoscopic spinal surgery
Exclusion Criteria
1) Patients with unstable cadiovascular status
2) Patients with acute infection
3) Patients with previous lumbar spinal surgery
4) Patients with anticoagulant or antiplatelet drugs
5) Patients who does not understand study protocol
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cervical epidural pressure
- Secondary Outcome Measures
Name Time Method visual analog scale, Oswestry Diability Index