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Lumbar Spinal Stenosis clinical trials

View clinical trials related to Lumbar Spinal Stenosis.

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NCT ID: NCT05147064 Not yet recruiting - Clinical trials for Lumbar Spinal Stenosis

Minimal Invasive Surgery Versus Interlaminar Decompression in Lumbar Canal Stenosis

Start date: December 1, 2021
Phase: N/A
Study type: Interventional

Conventional open surgery has been shown to be an effective procedure for LCS decompression. Minimally invasive surgery (MIS) through tubular retractors is a recently introduced alternative procedure for decompression of LCS. The current study aims at evaluating the efficacy of minimally invasive surgery as a decompressive procedure in comparison to conventional open surgery for the treatment of patients with LCS.

NCT ID: NCT04946487 Not yet recruiting - Clinical trials for Lumbar Spinal Stenosis

Effect of the Posterior Ligamentous Complex on the Adjacent Segments Degeneration After Lumbar Surgery

Start date: July 1, 2021
Phase:
Study type: Observational

To investigate whether destroying the adjacent posterior ligamentous complex (PLC) has an effect on adjacent segment degeneration (ASD) after L5/S1 posterior lumbar interbody fusion (PLIF)

NCT ID: NCT04778943 Not yet recruiting - Clinical trials for Lumbar Spinal Stenosis

Oblique Lateral Interbody Fusion Versus Minimally Invasive Transforaminal Lumbar Interbody Fusion

Start date: February 28, 2021
Phase:
Study type: Observational

The investigators will retrospectively study lumbar spinal stenosis patients who underwent OLIF or MIS-TLIF with percutaneous pedicle screw fixation between January 2016 and December 2019.The investigators will measure estimated blood loss, operative time, hospital stay, cost, reoperation, and complication incidence, visual analogue scale (VAS), Oswestry Disability Index (ODI), Japanese Orthopaedic Association (JOA), and Short Form-36 (SF-36) scores, discal and foraminal height, lumbar lordotic angle, and fusion status.The investigators will conduct to evaluate postoperative improvements, complications, and reoperation rates between patients with lumbar spinal stenosis (LSS) undergoing oblique lateral interbody fusion (OLIF) or minimally invasive transforaminal lumbar interbody fusion (MIS-TLIF).

NCT ID: NCT04341831 Not yet recruiting - Clinical trials for Lumbar Spinal Stenosis

Does Teicoplanin Powder Use In Lumbar Instrumentation Surgery Reduce Surgical Site Infection

Start date: April 15, 2020
Phase: Phase 3
Study type: Interventional

Infection after spinal surgery is one of the serious complications. Spinal surgery infection can cause high morbidity, mortality, and costs. In spite of different prophylactic methods, up to 15% of infection appears after spinal surgery. Vancomycin powder, which is one of the most applied methods, seems to be effective and inexpensive. However, vancomycin administration may be inconvenient in elderly participants with high comorbidity and especially kidney problems. The investigators aimed to reduce the rate of infection in the post-op 90-day period by adding per-op Teicoplanin powder onto the implant in participants scheduled for lumbar posterior instrumentation.

NCT ID: NCT04124146 Not yet recruiting - Clinical trials for Lumbar Spinal Stenosis

Long-term Evolution of Patients Suffering From Lumbar Canal Stenosis and Supported by Minimally Invasive Surgery: SUIVISTENO

SUIVISTENO
Start date: December 1, 2019
Phase:
Study type: Observational

describe the functional evolution of patients at more than 10 years post intervention. describe the evolution of pain, satisfaction, quality of life of patients to more than 5 years pot intervention.

NCT ID: NCT03918512 Not yet recruiting - Clinical trials for Lumbar Spinal Stenosis

Development and Validation of a Questionnaire for Assessing Activity Limitation in Patients With Lumbar Spinal Stenosis : The Cochin L3S Questionnaire

CL3S
Start date: March 1, 2020
Phase:
Study type: Observational

To develop and validate a questionnaire aiming at assessing specific activity limitation in patients with lumbar spinal stenosis (LSS).

NCT ID: NCT03867630 Not yet recruiting - Clinical trials for Lumbar Spinal Stenosis

The Effect of Additional Transforaminal Epidural Blocks in Percutaneous Epidural Neuroplasty

Start date: May 10, 2019
Phase:
Study type: Observational

Percutaneous epidural neuroplasty (PEN) is an effective interventional treatment for radicular pain. But in some cases with wire catheter like Racz catheter, contrast runoffs were not shown to the foramen. This study will show that contrast runoff will affect the results of PEN and in cases which contrast runoff are not shown, additional transforaminal epidural blocks will affect the results of PEN by reviewing medical record, retrospectively.

NCT ID: NCT03388307 Not yet recruiting - Clinical trials for Lumbar Spinal Stenosis

Unilateral Approach for Bilateral Decompression of Lumbar Canal Stenosis

Start date: January 15, 2018
Phase: N/A
Study type: Interventional

The purpose of this study was to compare standard open laminectomy with ULBD approach in regard to efficiency, safety, and clinical outcome.

NCT ID: NCT03365401 Not yet recruiting - Clinical trials for Lumbar Spinal Stenosis

Efficiency of Surgical Treatment for Lumbar Spinal Stenosis

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

Decompression surgery has proved to be effective for Lumbar Spinal Stenosis (LSS) with persistent pain. But the efficiency of the surgery for degenerated LSS remain uncertain and is the subject of this study. This is a multiple center open-label randomised trial. Patients were randomly allocated to surgical group or a nonoperative group. Because of the procedure , neither patients nor investigators were blinded. The primary outcome is the change of symptom measure by the Oswestry disability index 6, 12, and 24 months after procedure.