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Percutaneous disc decompression in patient with lumbar discogenic pain

Factors to predict successful outcome of percutaneous disc decompression using the navigable device (L’DISQ) in patient with lumbar discogenic pain

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0005967
Enrollment
100
Registered
2021-03-05
Start date
2021-02-26
Completion date
Unknown
Last updated
2021-03-22

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

The Catholic University of Korea, Seoul St. Mary's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Chronic pain due to lumbar discs over 3 months lumbar MRI data verified No effect on conservative treatment

Exclusion criteria

Exclusion criteria: No spine MRI Accompanying other causative disorders that may explain the symptoms infection tumor Blood clotting disease Unstable psychiatric illness Pregnant women, lactating women

Design outcomes

Primary

MeasureTime frame
Numeric rating score—

Secondary

MeasureTime frame
Oswestry disability index—

Countries

Korea, Republic of

Contacts

Public ContactJi Yeong Kim

The Catholic University of Korea, Seoul St. Mary's Hospital

Outcome results

None listed

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