Endoscopic Versus Conventional Lumbar Decompression for Lumbar Canal Stenosis

NCT07562035 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2026-05-01

No results posted yet for this study

Summary

This is a randomized controlled trial comparing interlaminar uniportal endoscopic bilateral lumbar decompression with conventional open laminectomy in patients with degenerative lumbar canal stenosis. The study aims to evaluate and compare clinical outcomes including pain relief, functional improvement, operative parameters, and recovery profile between both surgical techniques. Patients will be followed postoperatively for one day outcomes, one month, and six months to assess effectiveness and safety of each procedure.

Conditions

  • Lumbar Spinal Stenosis

Interventions

PROCEDURE

Interlaminar Uniportal Endoscopic Lumbar Decompression

Minimally invasive interlaminar uniportal endoscopic decompression of the lumbar spinal canal performed for treatment of degenerative lumbar spinal stenosis. The procedure aims to relieve neural compression while preserving posterior spinal structures and reducing tissue trauma compared to open surgery.

PROCEDURE

Open Lumbar Laminectomy

Standard open lumbar laminectomy performed for decompression of the spinal canal in patients with degenerative lumbar spinal stenosis. The procedure involves removal of posterior bony and ligamentous structures to relieve neural compression.

Sponsors & Collaborators

  • General Organization for Teaching Hospitals and Institutes

    collaborator OTHER
  • Ain Shams University

    lead OTHER

Principal Investigators

  • Mohammad Yousof Aboukila, MD · Ain Shams University, Faculty of Medicine, Department of Neurosurgery

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-06-11
Primary Completion
2026-02-26
Completion
2026-02-26

Countries

  • Egypt

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07562035 on ClinicalTrials.gov