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Comparative Study Between Lumbar Foraminal Stenosis Treatment Modalities

Management of Lumbar Foraminal Stenosis Using Unilateral Biportal Endoscopy Versus Conventional Open Spine Surgery

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06686407
Enrollment
32
Registered
2024-11-13
Start date
2024-11-30
Completion date
2026-10-31
Last updated
2024-11-13

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

Conditions

Lumbar Foraminal Stenosis

Brief summary

The goal of this clinical trial is to compare the clinical and radiological outcome of two different interventional techniques in lumbar foraminal stenosis decompression. The main questions it aims to answer are: Does minimally invasive techniques give better results than conventional techniques? Participants will: Undergo minimally invasive intervention using unilateral biportal endoscopy for lumbar foraminal stenosis decompression Undergo lumbar fusion for lumbar foraminal stenosis decompression Keep a diary of their symptoms and improvement of these symptoms

Detailed description

Lumbar foraminal stenosis decompression will be done using two different techniques: 1. Conventional Open Lumbar fusion By laminectomy and facetectomy and fixation with screws and rods ± interbody cage 2. Minimally invasive (Unilateral Biportal Endoscopy) Basic spine surgery instruments, 0° and 30° angled 4-mm diameter endoscopes commonly used in joint arthroscopic surgery, a radiofrequency catheter, Arthroscopic burr, and a shaver. Surgical approach to the foraminal area Two portals are created to perform this surgery. Water is infused through the endoscope through the viewing portal, and the working portal had an additional purpose as a portal for water outflow. The proximal and distal portals are created 2 cm lateral from the pedicle level on the C-arm anteroposterior image. Each incision for the portals is 0.8 cm in length, which is adequate for instrument and endoscope insertion. For the left side foramen, the proximal and distal portals are used as the viewing and working portals, respectively, and vice versa for the right foramen. After the endoscope insertion through the viewing portal, we secure a space for the lower transverse process around the lateral surface of the facet joint. A radiofrequency catheter or a shaver is used to secure the space, and a radiofrequency catheter is used to control active bleeding. Decompression of foraminal stenosis After a sufficient working space is obtained, the cranial 50% of the superior articular process of the thickened facet joint is removed using an arthroscopic burr or an osteotome. After removing the superior articular process, the ligamentum flavum around the foramen is removed using a curette and a Kerrison punch. After completion of flavectomy, nerve root and epidural fat are identified. If herniated disc material is found preoperatively, additional discectomy is performed usually from the axilla of the root. Surgery is confirmed to be completed after achieving an amount of free space concordant with the diameter of the nerve root in the foraminal zone, and then a drain tube is inserted.

Interventions

PROCEDUREOpen lumbar decompression ± fusion

Open lumbar decompression by laminectomy and transpedicular screw fixation using screws and rods ± interbody cage device

PROCEDUREMinimally invasive lumbar foraminal decompression using unilateral biportal endoscopy device

A new endoscopic technique that uses a Unilater Biportal Endoscopy for lumbar foraminal decompression

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* All Patients with degenerative lumbar foraminal stenosis, diagnosed in outpatient clinic. * Patients (age \>18 )

Exclusion criteria

* Deformity. * Infection of vertebrae. * Tumor of vertebrae. * Instability.

Design outcomes

Primary

MeasureTime frame
Oswestry disability index (ODI)Through study completion, an average of 2 years
Visual analogue scale (VAS)Through study completion, an average of 2 years

Secondary

MeasureTime frame
Post operative radiological assessment by MRI on lumbosacral spine.Through study completion, an average of 2 years

Contacts

Primary ContactAlaa Eldeen Mohamed Adam, Assistant lecturer
alaaoreaby@gmail.com+)201008798181
Backup ContactRadwan Nouby, Professor
+0201224480595

Outcome results

None listed

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