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Clinical efficacy and imaging comparison of modified W-TLIF versus P/TLIF in patients with single-level lumbar spinal stenosis: a randomized controlled study.

Clinical efficacy and imaging comparison of modified W-TLIF versus P/TLIF in patients with single-level lumbar spinal stenosis: a randomized controlled study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090053
Enrollment
Unknown
Registered
2024-09-23
Start date
2024-10-08
Completion date
Unknown
Last updated
2024-09-30

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

Conditions

lumbar spinal stenosis

Interventions

Experimental group:modified W-TLIF surgery
Control group:P/TLIF surgery

Sponsors

The First Affiliated Hospital of Dali University, Yunnan Province, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Chronic low back pain accompanied by lower limb nerve symptoms or intermittent claudication, which seriously affects daily life and work; (2) Ineffective after systematic conservative treatment, the time is = 3 months; (3) After a detailed medical history and physical examination before surgery, complete imaging data (bone density, X-ray, CT and MRI) were available; (4) Diagnosis of L4/5 or L5/S1 lumbar spinal stenosis requiring surgical treatment; (5) Patients with a follow-up time of = 1 year; (6) Patients who agree to the surgical plan;

Exclusion criteria

Exclusion criteria: (1) Incomplete preoperative data; (2) It is accompanied by other pathogenic factors such as trauma, tumor, and infection; (3) Exclusion of isthmus fissure-slip and severe degenerative scoliosis; (4) Lumbar spondylolisthesis above grade II; (5) Lost to follow-up with less than 1 year of follow-up.

Design outcomes

Primary

MeasureTime frame
time of operation;Intraoperative blood loss;Postoperative diversion;Postoperative hospital stay;adverse event;Visual analogue scores, VAS(lumbar pain);Visual analogue scores, VAS(leg pain);JOA score;(Oswestry disability index, ODI);Grade of muscle-fat infiltration;Skeletal Muscle Index, SMI;Intervertebral fusion evaluation system;

Secondary

MeasureTime frame
lumbar lordosis,LL;height of the intervertebral disc,HOD;Pelvic Incidence, PI;Pelvic Tilt, PT;Saccral Slope, SS;

Countries

China

Contacts

Public ContactRubin Yao

The First Affiliated Hospital of Dali University,

2226091078@qq.com+86 139 8724 8863

Outcome results

None listed

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