Clinical trial of custom-made titanium for cervical spine fusion

Clinical trial of custom-made titanium for cervical spine fusion - Clinical trial of custom-made titanium

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000009145

Enrollment

Registered

2012-11-01

Start date

2012-12-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

cervical spondylotic myelopathy, cervical disc hernia, cervical ossification of posterior ligamentum flavum, cervical spondylotic radiculopathy

Interventions

Anterior cervical fusion

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Cervical spondylotic myelopathy, cervical disc hernia, cervical ossification of posterior ligamentum flavum, cervical spondylotic radiculopathy. 2) Good general status

Exclusion criteria

Exclusion criteria: 1) No lumbar or thoracic spine disease 2) No collagen disease 3) No uncontrolable general disease 4) No malignacy 5) No psychological disease 6) No steroid treatment

Design outcomes

Primary

Measure	Time frame
Evaluation of adverse event and failure. Improvement of preoperative symptoms.	—

Countries

Japan

Contacts

Public ContactShunsuke Fujibayashi

Kyoto University Hospital Orthopaedic surgery

shfuji@kuhp.kyoto-u.ac.jp075-761-3652

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026