Efficacy of Navigable Percutaneous Plasma Disc Decompression Device (L'DISQ) in Patients With Severe Lumbar Disc Herniation
NCT05231759 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 30
Last updated 2022-02-09
Summary
This study aims to assess the clinical outcome of percutaneous disc decompression using the L'DISQ in patients with severe lumbar disc herniation (LDH).
Conditions
- Lumbar Disc Herniation
Interventions
- DEVICE
-
L'DISQ
Sponsors & Collaborators
-
Korea University Anam Hospital
lead OTHER
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-03-01
- Primary Completion
- 2019-02-28
- Completion
- 2022-03-31
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