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A prospective study of intervertebral fusion and disc removal in single-level TLIF surgery

A prospective study of intervertebral fusion and disc removal in single-level TLIF surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400093841
Enrollment
Unknown
Registered
2024-12-12
Start date
2024-01-17
Completion date
Unknown
Last updated
2024-12-16

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

Conditions

Degenerative lesions of the lumbar spine

Interventions

low-dose group:none
high-dose group:none

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Patients undergoing single-level TLIF surgery

Exclusion criteria

Exclusion criteria: (1) Patients with endplate inflammation Modic type III; (2) Bone mineral density T value <=-4.0; (3) Patients with previous lumbar deformity, tumor, surgery and infection; (4) Patients with intellectual disabilities, dementia and other diseases, or drug abuse who cannot cooperate with treatment.

Design outcomes

Primary

MeasureTime frame
Grading of interbody fusion;—

Secondary

MeasureTime frame
Preoperative and postoperative visual analogue pain score (VAS);Preoperative and postoperative Functional Impairment Index score (ODI);Preoperative and postoperative Japan Orthopaedic Society Lumbar Spine Score (JOA);Disc mass and volume;—

Countries

China

Contacts

Public ContactLitai Ma

Department of Orthopedics, West China Hospital, Sichuan University

ma.litai@163.com+86 189 8060 5820

Outcome results

None listed

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