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Clinical Study of Cement-Augmented Endplate Reinforcement in OLIF for Lumbar Spinal Stenosis with Osteoporosis

Clinical Study of Cement-Augmented Endplate Reinforcement in OLIF for Lumbar Spinal Stenosis with Osteoporosis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096319
Enrollment
Unknown
Registered
2025-01-21
Start date
2023-09-04
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Lumbar degenerative diseases

Interventions

OLIF-BCAAS:Undergoing Oblique lateral interbody fusion with bone cement-augmented anterolateral screws
OLIF-PIFPS:Undergoing Oblique lateral interbody fusion combined with posterior internal fixation with pedicle screws

Sponsors

The People's Hospital of Guangxi Zhuang Autonomous Region
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: a. Adult patients meet the diagnostic criteria for lumbar spinal stenosis combined with lumbar instability. b. Dual-energy X-ray indicates that the bone density T-score of the surgically responsible segment of the lumbar vertebrae is less than -2.5 standard deviations. c. There are surgical indications for single-segment lumbar fusion and a willingness to undergo surgery. d. Willing to participate in this study, fully informed and consent to the research content, and able to cooperate for evaluation and data collection at different follow-up points. e. The research will be conducted at the Department of Spinal Surgery, Guangxi Zhuang Autonomous Region People’s Hospital. The study period is from January 2024 to December 2026.

Exclusion criteria

Exclusion criteria: a. Not suitable for undergoing OLIF (Oblique Lumbar Interbody Fusion) due to conditions such as central canal stenosis of the lumbar spine, extruded intervertebral disc herniation, and grade II or higher spondylolisthesis. b. Multiple underlying diseases that make the patient unable to tolerate surgery/anesthesia. c. Concurrent presence of other conditions causing lumbar back pain, lower limb functional impairment, or other diseases that may affect the assessment of treatment efficacy.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale;Oswestry disability index;Japanese Orthopaedic Association scores;Interveterbral disc height;

Secondary

MeasureTime frame
Operation duration;Intraoperative blood loss;Length of surgical incision;Duration of hospitalization;Complications;

Countries

China

Contacts

Public ContactWei Jianxun

The People's Hospital of Guangxi Zhuang Autonomous Region

jxwei1972@163.com+86 771 218 6685

Outcome results

None listed

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