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Lumbar Spinal Stenosis clinical trials

View clinical trials related to Lumbar Spinal Stenosis.

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NCT ID: NCT05523388 Recruiting - Clinical trials for Lumbar Spinal Stenosis

Role of Spinal Load in the Pathophysiology of Lumbar Spinal Stenosis

RoLSSroice
Start date: September 1, 2022
Phase:
Study type: Observational

This study is to improve the understanding of the role of postural and ambulatory biomechanics for symptoms in patients with sLSS and to correlate patient-reported outcome measures (PROMs) with dynamic compensation (difference between static and dynamic sagittal spinal alignment) in patients with symptomatic lumbar spinal stenosis sLSS).

NCT ID: NCT05504499 Recruiting - Clinical trials for Lumbar Spinal Stenosis

REFINE Study: A Study In a Novel Interspinous Fusion Device In Subjects With Low Back Pain

Refine
Start date: March 19, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effectiveness and safety of the use of Aurora Spine ZIP™ MIS Interspinous Fusion System and bone graft material in fusion in patients with chronic low back pain that present with degenerative disc disease with concurrent neurogenic claudication.

NCT ID: NCT05447780 Recruiting - Clinical trials for Lumbar Spinal Stenosis

Comparing General Anesthesia, General Anesthesia With ESP Block or TLIP Block in Patients Undergoing Lumbar Surgeries

Start date: April 18, 2022
Phase: N/A
Study type: Interventional

The regional methods of anesthesia for the neurosurgical operations of the spine and spinal cord reducing the needs for opioids intra operatively and reducing pain in the postoperative period, decrease the numbers of failed back syndrome.

NCT ID: NCT05425667 Recruiting - Clinical trials for Lumbar Spinal Stenosis

Sensory Integration Therapy Training in Patients With Lumbar Spinal Stenosis

Start date: April 15, 2021
Phase: N/A
Study type: Interventional

Lumbar spinal stenosis is a common degenerative disease in the elderly. Patients are often accompanied by paresthesias and decreased musculoskeletal system functions, resulting in disability and increasing the burden of medical care. The balance and walking ability of such patients are affected by the compressed nerves, so it is necessary to reorganize the nerve sensory systems to compensate for the disability caused by lumbar stenosis. It is necessary to strengthen the training of sensory integration ability, but it has not been Studies have investigated which treatments or surgery can improve sensory integration in patients with lumbar stenosis. Therefore, this study will develop a clinical tool to objectively evaluate sensory integration, quantify the sensory integration ability of patients with lumbar stenosis and neurological claudication; The influence and mechanism of the balance ability.

NCT ID: NCT05403775 Recruiting - Clinical trials for Lumbar Spinal Stenosis

Application of 3D Printing Guide Plate in Dorsal Root Ganglion Intervention Treatments

Start date: July 8, 2022
Phase: N/A
Study type: Interventional

This study applies 3D-printed customized guide plate in assisting the accurate puncture in transforaminal epidural steroid injection (TFESI) combined with pulsed radiofrequency (PRF) treatment. This technique can shorten reduce the intra-operative radiation, and do not affect the surgical outcome.

NCT ID: NCT05073081 Recruiting - Clinical trials for Lumbar Spinal Stenosis

Feasibility of Prehab for Lumbar Spinal Stenosis

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

The literature has shown evidence of the effectiveness of prehabilitation programs on post-operative recovery for musculoskeletal conditions; however, evidence for prehabilitation for lumbar spinal stenosis (LSS) is limited. Investigators have found that there is very low to low quality evidence for the effect of prehabilitation interventions for improving outcomes following lumbar spine surgery. Therefore, the purpose of this study will be to determine the feasibility of a prehabilitation program for patients undergoing LSS surgery, and pilot test the protocol to provide the foundation for future design of a larger, multicenter randomized controlled trial.

NCT ID: NCT05058287 Recruiting - Pain, Postoperative Clinical Trials

Lumbar Steroid Use in Patients Undergoing Posterior Lumbar Decompression

Start date: November 5, 2021
Phase: Phase 3
Study type: Interventional

This study seeks to evaluate the impact of intra-operative topical epidural steroid usage in patients undergoing 1-2 level lumbar laminectomy. The study will examine post-operative opioid usage, length of stay, return to work, and patient reported outcomes following these procedures.

NCT ID: NCT05029726 Recruiting - Clinical trials for Degenerative Disc Disease

Regional Anesthesia in Minimally Invasive Lumbar Spine Surgery

Start date: February 1, 2022
Phase: Phase 4
Study type: Interventional

Opioid overuse is a widespread public health crisis in the United States with increasing rates of addiction and overdose deaths from prescription opioids. Reducing the need for opiate analgesics in the post-operative setting has become a high priority in minimizing long-term opioid use in surgical patients. This study will serve to demonstrate the efficacy of the addition of regional analgesic techniques in reducing post-operative opioid requirements in patients undergoing common lumbar spinal surgical procedures.

NCT ID: NCT05023733 Recruiting - Clinical trials for Degenerative Disc Disease

Clinical and Radiographic Outcomes of TLIF w/3D Printed Cellular Implant

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

This study is designed to evaluate clinical outcomes and spine fusion rates for patients undergoing transforaminal lumbar interbody fusion using the CONDUIT 3D printed titanium TLIF cage.

NCT ID: NCT04992572 Recruiting - Clinical trials for Lumbar Spinal Stenosis

Study Comparing Local/ MAC Anesthesia in Lumbar Decompression

Start date: December 1, 2021
Phase: Early Phase 1
Study type: Interventional

Explore efficacy, complications, and other factors associated with anaesthetic choice- To evaluate the efficacy of local + MAC as an alternative anesthetic to general anesthesia and to analyze patients' outcomes and experiences.