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Lumbar Discopathy Decompression with Lateral Interbody Fusion: Radiological and Clinical Outcomes

Single-Level Lateral Lumbar Interbody Fusion in Author's Modification: Clinical and Radiographic Outcomes

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06719349
Enrollment
38
Registered
2024-12-05
Start date
2021-01-01
Completion date
2021-12-31
Last updated
2024-12-05

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

Conditions

Fusion of Spine (Disease), Spine Degeneration

Keywords

Spine, Decompression, Interbody Fusion, Diskectomy

Brief summary

The aim of the study was to introduce a single-segment lumbar spine decompression and fusion with intervertebral implants through modified by the authors lateral lumbar approach. Functional, surgical and radiographic outcomes was evaluated.

Interventions

None listed

Sponsors

Podkarpackie Oncological Center
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

Single-segment L1-L4 spine discopathy.

Exclusion criteria

Any other spinal diseases. More than one level of discopathy.

Design outcomes

Primary

MeasureTime frameDescription
the quality of life3 months after the surgerythe quality of life according to the EQ-VAS - Euro-Quality of Life Visual Analoque Score
the functional status - Karnofsky scale3 months after the surgerypatients' neurological status, functional status according to the Karnofsky scale
the functional status Oswestry Disability Index3 months after the surgerypatients' neurological status, functional status according to the ODI - Oswestry Disability Index
the intensity of pain3 months after the surgerythe intensity of pain according to the VAS - Visual AnalogueScale score

Secondary

MeasureTime frameDescription
Radiographic Outcomes: The Height and Width of the Intervertebral Foramina3 months after the surgeryBased on pre- and postoperative MRI/RTG the following aspects were assessed: The Height and Width of the Intervertebral Foramina
Radiographic Outcomes: lumbar segmental angle.3 months after the surgeryBased on pre- and postoperative MRI/RTG the following aspects were assessed: lumbar segmental angle.
Radiographic Outcomes: The Cross-Sectional Area of the Spinal Canal3 months after the surgeryBased on pre- and postoperative MRI/RTG the following aspects were assessed: The Cross-Sectional Area of the Spinal Canal, the width and depth of disc extrusion, and the width of the lateral recesses of the spinal canal, anterior disc height lumbar lordosis angle and lumbar segmental angle.

Countries

Poland

Outcome results

None listed

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