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Comparison of the clinical efficacy of Endo-TLIF with traditional posterior lumbar interbody fusion in the treatment of single-level degenerative lumbar spondylolisthesis

Comparison of the clinical efficacy of Endo-TLIF with traditional posterior lumbar interbody fusion in the treatment of single-level degenerative lumbar spondylolisthesis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096910
Enrollment
Unknown
Registered
2025-02-08
Start date
2025-02-10
Completion date
Unknown
Last updated
2025-02-17

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

Conditions

Degenerative lumbar spondylolisthesis

Interventions

Group of Endoscopic:Endo-TLIF
Group of Open Treatment:Posterior lumbar interbody fusion

Sponsors

Weifang People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Lumbar X-ray, CT and MRI confirmed Meyerding classification I.°~II.° single-level degenerative lumbar spondylolisthesis; 2. Recurrent or persistent onset of low back pain and/or leg pain or intermittent claudication, and the lesion segment is consistent with the imaging manifestations; 3. The course of the disease is more than 3 months and the symptoms cannot be alleviated after strict conservative treatment, which seriously affects work and daily life; 4. Patients undergoing elective Endo-TLIF surgery or posterior lumbar interbody fusion; 5. All patients were performed by the same group of senior physicians.

Exclusion criteria

Exclusion criteria: 1. Those who do not meet the above inclusion criteria; 2. Those who have a history of relevant lumbar spine surgery in the past; 3. Patients with infection of adjacent tissues of the lumbar spine; 4. Patients with severe spinal deformity (Cobb angle above 20 degrees) or osteoporosis (T value <-2.5); 5. Patients with severe systemic diseases or internal organ dysfunction that cause inability to tolerate surgery or anesthesia; 6. Patients with multi-level lumbar spondylolisthesis; 7. Those with severe mental or cognitive impairment; 8. Advanced malignant tumor.

Design outcomes

Primary

MeasureTime frame
Duration of surgery;Intraoperative blood loss;Postoperative drainage;Length of hospital stay;Low back pain visual analogue scale score;Lower limb pain visual analogue scale score;Oswestry Dability Index;

Countries

China

Contacts

Public ContactBinwu Wang

Weifang People's Hospital

bwwspine@126.com+86 137 9162 9600

Outcome results

None listed

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