Comparison of the stability of the porous structure of 3D printed Ti and conventional PEEK intervertebral fusion prosthesis in spinal surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0006624

Enrollment

Registered

2021-09-30

Start date

2021-09-30

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

Medical Device : Block randomization and randomized control trials are planned for osteoporosis patients who underwent posterior decompression and interbody fusion for lumbar degenerative disease. It

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: - Patients over 20 years of age who are scheduled to undergo posterior spinal instrumentation due to degenerative diseases of the lumbar spine - Patients who have not responded to conservative treatment for more than 6 months due to lumbar spinal stenosis, spondylolisthesis, or repeated lumbar disc herniation - Patients with osteoporosis (T score = -2.5) in the lumbar spine and femoral bone density test. - Patients who voluntarily consented in writing to participate in this clinical trial

Exclusion criteria

Exclusion criteria: -Patients undergoing spinal instrumentation after being infectious status from spinal or intervertebral disc and tumorous status from vertebral body and spinal cord -Patients who do not consent to the study -Patients judged unsuitable for participation in clinical trials by other investigators

Design outcomes

Primary

Measure	Time frame
fusion rate	—

Secondary

Measure	Time frame
complication rate	—

Countries

Korea, Republic of

Contacts

Public ContactJiwon Kwon

Yonsei University Health System, Gangnam Severance Hospital

kwonjjanng@yuhs.ac+82-2-2019-3411

Outcome results