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Spinal Stenosis clinical trials

View clinical trials related to Spinal Stenosis.

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NCT ID: NCT05035693 Recruiting - Radiculopathy Clinical Trials

Post Market Clinical Follow up Study With the Cervical Disc Prothesis MOVE®-C

PMCF_MOVE®-C
Start date: March 11, 2021
Phase: N/A
Study type: Interventional

Study design: International, prospective, multicentre, non-randomised, observational study according to § 23b MPG. Objectives: Observational study to confirm the safety and performance of the cervical disc prosthesis MOVE®-C.

NCT ID: NCT05033457 Enrolling by invitation - Clinical trials for Lumbar Disc Herniation

Comparative Study Between UBE and PETD for the Treatment of Lumbar Spinal Canal Stenosis

Start date: January 1, 2018
Phase:
Study type: Observational

OBJECTIVE Both unilateral biportal endoscopy technique(UBE) and percutaneous endoscopic transforaminal discectomy(PETD) are minimally invasive and effective surgical procedures for lumbar spinal stenosis.The object of this retrospective study was to compare the clinical and radiological outcomes between UBE and PETD. METHODS In the period from July 2020 to December 2020, using UBE or PETD to treat lumbar canal stenosis.Patients were classified into two groups based on the surgery they had undergone. Preoperative and postoperative MR image was used to evaluate the removal rate of lumbar disc herniated material by two surgical methods. The two surgical methods are also compared and evaluated in terms of operation time, incision size, hospitalization time, etc.

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.

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: NCT04876612 Recruiting - Clinical trials for Lumbar Spinal Stenosis

Effect of Limaprost in Combination With Transforaminal Epidural Steroid Injection

Start date: November 10, 2021
Phase: N/A
Study type: Interventional

The purpose of this study was to compare the effects of limaprost(Opalmon® ) on walking ability, low back pain and leg pain after transforaminal epidural steroid injection (TFESI) was administered compared to the placebo group.

NCT ID: NCT04839783 Recruiting - Clinical trials for Degenerative Disc Disease

Single Position Spine Surgery Registry

SPSG Registry
Start date: July 7, 2020
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to systematically, prospectively compare surgical fusion techniques for thoracolumbar spinal fusion patients and assess long-term patient outcomes and revision rates following surgery.

NCT ID: NCT04795284 Recruiting - Clinical trials for Lumbar Spinal Stenosis

Biomechanical Parameters of Gait in Patients With Symptomatic Lumbar Spinal Stenosis and Healthy Elderly.

Start date: September 9, 2020
Phase:
Study type: Observational

The aim of this study is to compare biomechanical walking parameters between patients with symptomatic lumbar spinal stenosis and healthy elderly.

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).