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Measuring cervical epidural pressure in biportal endoscopic spinal surgery

Measuring cervical epidural pressure in biportal endoscopic spinal surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0004075
Enrollment
10
Registered
2019-06-19
Start date
2019-05-31
Completion date
Unknown
Last updated
2019-07-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Korea University Anam Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Cervical epidural pressure—

Secondary

MeasureTime frame
visual analog scale, Oswestry Diability Index—

Countries

Korea, Republic of

Contacts

Public ContactTaewook Kang

Korea University Anam Hospital

taewook83@naver.com+82-2-920-5924

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026