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Using MRI scans to see how small-cut spine surgery improves space for nerves in the lower back

Quantitative MRI assessment of lumbar dural sac area following minimally invasive transforaminal lumbar interbody fusion: a retrospective single-center study - NIL

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/12/099006
Enrollment
200
Registered
2025-12-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: M480- Spinal stenosis

Interventions

Intervention1: Nil: Nil

Sponsors

Stavya Spine Hospital and Research Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Undergoing single-level MIS-TLIF for degenerative lumbar conditions (e.g., spinal stenosis, low-grade spondylolisthesis) at SSHRI during the study period. 2. Availability of high-quality lumbar MRI scans both before and after surgery (axial T2 sequences at the fused level). 3.Minimum radiographic follow-up of 6 months.

Exclusion criteria

Exclusion criteria: 1. History of prior lumbar spine surgery at the index or adjacent levels. 2. Surgery for non-degenerative pathology (e.g., tumor, infection, trauma). 3. Multi-level fusion procedures (more than one operative level). 4. Incomplete clinical records or missing imaging data at required time points. 5. Contraindications to MRI (e.g., incompatible implants), resulting in no postoperative MRI.

Design outcomes

Primary

MeasureTime frame
The following outcome measures will be recorded from each patient s chart and imaging studies: Dural sac area (mm ): Measured on axial T2-weighted MRI at the level of surgery (and adjacent levels). Canal diameters (mm): Anteroposterior and transverse diameters of the spinal canal on axial MRI. Clinical scores: Pre- and postoperative pain (VAS) and disability (ODI) if documented. Complications: Any intraoperative or postoperative adverse events noted in records Timepoint: Postoperative follow-up imaging included routine standing radiographs at 3 and 12 months to assess alignment and fusion, and MRI as clinically indicated. The primary imaging endpoint for this study is the postoperative MRI, which is usually obtained at approximately 6 12 months after surgery to evaluate nerve decompression and canal status.

Secondary

MeasureTime frame
NIL.Timepoint: NIL.

Countries

India

Contacts

Public ContactDr Bharat R Dave

Stavya Spine Hospital And Research Institute

brd_172@yahoo.com09825019913

Outcome results

None listed

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