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Spinal Stenosis clinical trials

View clinical trials related to Spinal Stenosis.

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NCT ID: NCT03381677 Suspended - Clinical trials for Lumbar Spinal Stenosis

Pedicle Osteotomy for Stenosis Trial

POST
Start date: October 26, 2017
Phase: N/A
Study type: Interventional

This is a pivotal Randomized Clinical trial to compare the safety and effectiveness of the Pedicle Lengthening Osteotomy Procedure with implantation of the Altum® Device to open surgical decompression and Transforaminal Lumbar Interbody Fusion (TLIF) in patients with symptomatic, one or two level lumbar spinal stenosis (LSS) and one level grade I degenerative spondylolisthesis requiring surgical treatment.

NCT ID: NCT03368638 Completed - Clinical trials for Lumbar Spinal Stenosis

Physical Therapy Treatments, Including Neural Mobilization and Hip/Back Stretches for People Between 50-89 With Lumbar Spinal Stenosis and Leg Pain Provoked by Walking

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

Aging of the back is common in the older people and can result in difficulties standing and walking. Conservative treatment is recommended before considering surgery. Some recommended exercises involve the use of expensive equipment. The present study plans to evaluate if specifically moving the nerves in the legs/back and improving flexibility of the hip and back can benefit patients. These exercises require no equipment, are simple to perform, and can provide patients a way to continue to perform these exercises at home. The purposes of this study are to (1) observe the benefit of a treatment program involving moving the nerves of the leg/back, stretching the legs and low back in patients with low back pain and difficulties walking; and (2) determine if benefits received remain at a 3-month follow-up.

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.

NCT ID: NCT03337178 Recruiting - Clinical trials for Lumbar Degenerative Spinal Stenosis

Fitbit Pilot Study in Post-operative Lumbar Degenerative Spinal Stenosis Patients

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

Spinal stenosis is a common orthopedic spine condition that limits individuals ability to walk and stand because of nerve compression. Surgical treatment can alleviate leg pain and improve function such as increasing physical activity. This study will use Fitbit technology to monitor patient's post-operative physical activity. It will evaluate the efficacy of a Fitbit incentive based walking program on improving post-operative physical activity and rehabilitation.

NCT ID: NCT03325309 Completed - Clinical trials for Lumbar Spinal Stenosis

Barriers and Facilitators to Cycling for Lumbar Spinal Stenosis

FLEXCAL Pilot
Start date: August 29, 2016
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether a home-based cycling program for patients with lumbar spinal stenosis is a feasible and acceptable

NCT ID: NCT03321357 Completed - Clinical trials for Degenerative Disc Disease

Retest-reliability and At-home-assessment Feasibility of the 5R-STS

5RSTS-2
Start date: December 8, 2017
Phase:
Study type: Observational

The five-repetition sit-to-stand test has been validated and is used primarily in pulmonary medicine and cardiology, and has recently been shown to be a useful tool for the objective assessment of functional impairment in patients with degenerative diseases of the lumbar spine. The goal of this study is to assess the possibility of supervised and unsupervised at-home-assessment. Validation of at-home-assessment would allow the 5R-STS to be easily used as a follow-up tool in clinical trials, for example.

NCT ID: NCT03303300 Completed - Clinical trials for Degenerative Disc Disease

The Five-repetition Sit-to-stand Test for Lower Back Pain or Radiculopathy

5R-STS
Start date: October 1, 2017
Phase: N/A
Study type: Observational

The five-repetition sit-to-stand test (5R-STS) has been used in many medical disciplines, but has never been correlated with or validated in regard to degenerative spinal diseases. The investigators aim to assess the possibility of using the standardized 5R-STS as an objective measure of functional impairment and pain severity in patients with degenerative lumbar spinal diseases.

NCT ID: NCT03302520 Completed - Clinical trials for Degenerative Lumbar Spinal Stenosis

Comparison of Bioactive Glass Ceramics Spacer and PEEK Cages in Posterior Lumbar Interbody Fusion: A Prospective, RCT

Novomax
Start date: October 28, 2017
Phase: N/A
Study type: Interventional

The authors aimed to compare the clinical efficacy and safety of CaO-SiO2-P2O5-B2O3 glass ceramics with PEEK cage that is widely used for posterior lumbar interbody fusion (PLIF) surgery in the clinical field.

NCT ID: NCT03302507 Completed - Clinical trials for Degenerative Lumbar Spinal Stenosis

Biportal Endoscopy Spine Surgery (BESS )Versus Unilateral Laminotomy Bilateral Decompression (ULBD ): RCT, Non-inferiority Trial

Start date: November 1, 2017
Phase: N/A
Study type: Interventional

This study is to compare the clinical outcome between the biportal endoscopic decompression and the unilateral approach bilateral decompression in spinal stenosis

NCT ID: NCT03245671 Withdrawn - Clinical trials for Lumbar Spinal Stenosis

Particulate vs. Nonparticulate Epidural Steroid Injections for Lumbar Foraminal Stenosis

Start date: December 2017
Phase: Phase 4
Study type: Interventional

Chronic lumbosacral radiculopathy secondary to lumbar spinal stenosis affects a large number of individuals, and there is a general lack of consensus in the medical community in terms of effective treatments for this problem. By assessing the relative efficacy of transforaminal epidural injections of particulate and nonparticulate steroids, this study attempts to further define the appropriate conservative management of painful unilateral radiculopathies due to unilateral lumbar foraminal stenosis. Patients will be randomized to receive a transforaminal epidural injection of either a particulate (Kenalog) or nonparticulate (Decadron) steroid. Outcomes will be assessed at 2 weeks, 6 weeks, 3 months, and 6 months following the injection.