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Analysis of clinical results of Biportal Endoscopic Spinal Surgery(BESS) in degenerative spinal stenosis of the lumbar spine. (A Prospective study)

Analysis of clinical results of Biportal Endoscopic Spinal Surgery(BESS) in degenerative spinal stenosis of the lumbar spine. (A Prospective study)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0006631
Enrollment
108
Registered
2021-10-01
Start date
2021-10-11
Completion date
Unknown
Last updated
2021-10-05

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

Chungnam National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ? Adults 19 years of age or older ? In case of degenerative spinal stenosis of the lumbar spine according to physical examination and radiology examination, one of the following a-c a) Simple degenerative spinal stenosis or b) degenerative spinal stenosis of the lumbar spine with degenerative spondylolisthesis or c) degenerative spinal stenosis of the lumbar spine with degenerative scoliosis ? Patients with degenerative spinal stenosis who have undergone conservative treatment (medication, physical therapy, selective nerve root block, etc.) for more than 3 months but failed to control symptoms and are scheduled to undergo decompression surgery using a two-way endoscope ? Subjects who agreed to complete the survey because it was possible to follow up for 24 months before and after surgery

Exclusion criteria

Exclusion criteria: ? Patients who did not faithfully respond to the questionnaire after surgery or did not complete the questionnaire during the period of participation in this study ? Patients who currently have a mental illness, such as delirium/dementia, or who have progressed to the disease during the participation period, and are judged to be difficult to cooperate with in this clinical trial. ? If the patient does not agree to participate in the study ? Other patients who are judged unsuitable for clinical research by the person in charge of clinical research.

Design outcomes

Primary

MeasureTime frame
Radiological examination (simple radiography and magnetic resonance examination) and visual analogue scale (VAS), Oswestry disability index (ODI), health-related quality of life measurement tool (EQ-5D), surgery Post-satisfaction (modified Macnab criteria)

Secondary

MeasureTime frame
Radiological examination (simple radiography and magnetic resonance examination) and visual analogue scale (VAS), Oswestry disability index (ODI), health-related quality of life measurement tool (EQ-5D), surgery Post-satisfaction (modified Macnab criteria)

Countries

Korea, Republic of

Contacts

Public ContactHOJIN LEE

Chungnam National University Hospital

leeleo98@gmail.com+82-42-280-7342

Outcome results

None listed

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