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Assessing Risk Factors for Radiological Complications After Transforaminal Lumbar Interbody Fusion

AgeTLIF - Assessing Risk Factors for Radiological Complications After Transforaminal Lumbar Interbody Fusion

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05266638
Acronym
AgeTLIF
Enrollment
170
Registered
2022-03-04
Start date
2022-01-19
Completion date
2023-02-15
Last updated
2024-02-20

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

Conditions

Degenerative Lumbar Spine Diseases

Keywords

Posterior Lumbar Interbody Fusion (PLIF), Transforaminal Lumbar Interbody Fusion (TLIF), Implant Failure, Revision Surgery

Brief summary

This retrospective study is to determine whether age is a risk factor for postoperative complications in patients undergoing transforaminal lumbar interbody fusion; specifically whether the risk (odds) of implant failure and the need for revision surgery increases with age.

Detailed description

Spinal fusion is one of the most commonly performed surgical procedures for the treatment of degenerative spinal disease. Interbody fusion with cages reconstructs the anterior column through disc removal, allowing to maintain proper disc height despite weight bearing, while providing firm fixation of the spinal segments. Transforaminal lumbar interbody fusion (TLIF) has fewer complications and less intraoperative bleeding than posterior lumbar interbody fusion (PLIF). Elderly patients are at high risk for perioperative and postoperative complications after lumbar fusion. This retrospective study is to determine whether age is a risk factor for postoperative complications in patients undergoing transforaminal lumbar interbody fusion; specifically whether the risk (odds) of implant failure and the need for revision surgery increases with age.

Interventions

OTHERData collection (radiological parameters, outcome information) from electronic patient files in hospital data system

Collection of medical data and medical images (MRI, radiographs) of the lumbar spine and pelvis of patients having received TLIF with degenerative spinal diseases from the years 2015-2020 and statistical analysis of the coded data.

Sponsors

University Hospital, Basel, Switzerland
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Indications for TLIF surgery (e.g., degenerative disc disease, spondylolisthesis) * Existing preoperative upright standing sagittal plane X-ray of lumbar spine with clear visibility of pelvis, sacrum and femoral head * Existing preoperative MRI of the lumbar region with clear visibility of different fatty infiltration grade and stenosis degree * Complete follow-up at 3 months and 1 year postoperatively, including clinical and radiographic data

Exclusion criteria

* Neuromuscular diseases such as Parkinson's disease or multiple sclerosis according to our records * Preoperative infection and/or malignancy tumor with involvement of the bony or soft tissue structures of the lumbar spine * Presence of a documented consent dissent

Design outcomes

Primary

MeasureTime frameDescription
Number of Implant failureone time assessment at baselineNumber of Implant failure (screw loosening, cage subsidence, adjacent level alteration/ degeneration, spondylolisthesis degree, kyphosis of the adjacent intervertebral disc space, reduced height of intervertebral disc space) in relationship to age
Number of patients needing revision surgeryone time assessment at baselineNumber of patients needing revision surgery, in relationship to age

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026