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Radiological investigation of lumbar lordosis after single level MIS TLIF :Prebent rods ideal or not

Are prebent rods ideal: a radiological analysis of lumbar lordosis after single level MIS TLIF at L3-4, L4-5, and L5-S1 - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/01/061238
Enrollment
385
Registered
2024-01-08
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: M404- Postural lordosis

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Stavya Spine Hospital and Research Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing a single-level Minimally invasive TLIF procedure for the treatment of a single-level degenerative lumbar condition will be included in the study.

Exclusion criteria

Exclusion criteria: Patients undergoing more than one level of surgery Patients undergoing fusion for a non-degenerative condition(deformity, tumor, trauma or infection) Patients undergoing fusion for high-grade spondylolisthesis

Design outcomes

Primary

MeasureTime frame
Lordosis of prebent rod Total Lumbar Lordosis - pre-operative and post-operative (Day 3) Segmental Lordosis achieved at the fusion levelTimepoint: No follow up visit—

Secondary

MeasureTime frame
NATimepoint: NA—

Countries

India

Contacts

Public ContactDr Bharat R Dave

Stavya Spine Hospital And Research Institute

brd_172@yahoo.com9825019913

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 27, 2026