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Application of cortical screw fixation in posterior lumbar interbody fusion

Application of cortical screw fixation in posterior lumbar interbody fusion

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900022658
Enrollment
Unknown
Registered
2019-04-20
Start date
2019-05-01
Completion date
Unknown
Last updated
2019-04-23

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

Conditions

Lumbar degenerative disease

Interventions

Experimental group:MIDLF
control group:PLIF/TLIF

Sponsors

Beijing Chaoyang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: At least 18 years of age; at least 3 months of conservative treatment failure, only chronic low back pain or associated with lower limb nervous system symptoms; single or multi-segment TLIF and PLIF indications (including lumbar spondylolisthesis, lumbar disc herniation, lumbar disc Degenerative changes, etc.).

Exclusion criteria

Exclusion criteria: Patients who cannot tolerate surgery; patients with coagulopathy; active infections; patients with grade III and IV lumbar spondylolisthesis according to Meyerding classification; immigrant planners within 3 years after enrollment; pregnant patients; patients with metabolic bone disease; Patients treated with glucocorticoids or immunosuppressive agents.

Design outcomes

Primary

MeasureTime frame
VAS score;Oswestry Disability Index;Blood creatine kinase concentration immediately after surgery;operation time;blood loss during operation;fusion rate;

Countries

China

Contacts

Public ContactLiu Yuzeng
beijingspine2010@163.com+86 13811552832

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026