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Effectiveness and safety of SPINOFILL® in patients with osteoporotic compression fracture

Effectiveness and safety of SPINOFILL® in patients with osteoporotic compression fracture

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0005425
Enrollment
37
Registered
2020-09-23
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-10-05

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

Gachon University Gil Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Adult age (19-100) with osteoporosis 2) Persistent severe pain despite adequate conservative treatment at least 2 weeks 3) 7 or more of visual analogue scale (VAS) 4) 20 or more of Oswestry Disability Index (ODI) 5) Patients with voluntary consent

Exclusion criteria

Exclusion criteria: 1) Contraindication of vertebroplasty 2) Patients who do not agree to participate in the study

Design outcomes

Secondary

MeasureTime frame
Complication of SPINOFILL—

Primary

MeasureTime frame
The degree of pain improvement—

Countries

Korea, Republic of

Contacts

Public ContactSeong Son

Gachon University Gil Medical Center

Outcome results

None listed

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