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Comparison of the Clinical Outcomes between the Modified MIS-TLIF with Freehand Screw Placement and Traditional MIS-TLIF in Lumbar Spine Surgery

Comparison of the Clinical Outcomes between the Modified MIS-TLIF with Freehand Screw Placement and Traditional MIS-TLIF in Lumbar Spine Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400094735
Enrollment
Unknown
Registered
2024-12-26
Start date
2023-03-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Degenerative lumbar disease

Interventions

modified MIS-TLIF group:This group of patients underwent modified MIS-TLIF.
MIS-TLIF group:This group of patients underwent MIS-TLIF.

Sponsors

Southwest Hospital, Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1.Diagnosed with lumbar degenerative diseases, including lumbar disc herniation, lumbar spinal stenosis, or lumbar spondylolisthesis; 2.Patients who showed no improvement after three months of conservative treatment, undergoing their first surgical intervention with single-level MIS-TLIF or MMIS-TLIF procedures; 3.Follow-up period of at least 12 months.

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1.History of prior lumbar surgery; 2.Patients with trauma, active infection, malignancy, spinal deformity, or previous lumbar fusion and multilevel fusion surgeries.

Design outcomes

Primary

MeasureTime frame
Intraoperative blood loss;Operative time;Fluoroscopy time;The amount of blood transfused;Complications;Preoperative Back pain VAS(Visual Analogue Scores) scores ;Preoperative Lower limb pain VAS(Visual Analogue Scores) scores;Preoperative ODI(Oswestry Disability Index);Preoperative JOA(Japanese Orthopaedic Association Scores) scores;Preoperative Fatty infiltration of multifidus Ratio;3 Days postoperative Back pain VAS(Visual Analogue Scores) scores ;3 Months postoperative Back pain VAS(Visual Analogue Scores) scores ;6 Months postoperative Back pain VAS(Visual Analogue Scores) scores ;12 Months postoperative Back pain VAS(Visual Analogue Scores) scores ;3 Days postoperative Lower limb pain VAS(Visual Analogue Scores) scores;3 Months postoperative Lower limb pain VAS(Visual Analogue Scores) scores;6 Months postoperative Lower limb pain VAS(Visual Analogue Scores) scores;12 Months postoperative Lower limb pain VAS() scores;3 Months postoperative ODI(Oswestry Disability Index);6 Months postoperative ODI(Oswestry Disability Index);12 Months postoperative ODI(Oswestry Disability Index);3 Months postoperative JOA(Japanese Orthopaedic Association Scores) scores;6 Months postoperative JOA(Japanese Orthopaedic Association Scores) scores;12 Months postoperative JOA(Japanese Orthopaedic Association Scores) scores;Fusion 6 months after surgery;Fusion 12 months after surgery;12 Months postoperative Fatty infiltration of multifidus Ratio;

Secondary

MeasureTime frame
Age;Gender;Number of days in hospital;Number of days of postoperative hospital stay;Etiologys;Surgical segment;

Countries

China

Contacts

Public ContactZehua Zhang

Southwest Hospital, Army Medical University

zhangzehuatmmu@163.com+86 132 4351 7375

Outcome results

None listed

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