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Spinal Stenosis clinical trials

View clinical trials related to Spinal Stenosis.

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NCT ID: NCT04193488 Completed - Postoperative Pain Clinical Trials

Mid-Transverse Process to Pleural (MTP) Block and Erector Spinal Plan (ESP) Block in Spinal Surgery

Start date: October 23, 2019
Phase: N/A
Study type: Interventional

Ethics committee approval was taken on October 22, 2019, numbered 19/342. 120 adult patients who will undergo spine stabilization surgery between October 2019 and January 2020 in "Gülhane Training and Research Hospital" were planned to be included in the study. Patients will be randomized to 30 patients with MTP block (Group MTP) and ESP block (Group ESP) and no block (Group K) in addition to patient-controlled analgesia (PCA). Postoperative pain scores, analgesic use, number of PCA button presses, total amount of opioid administered and complications due to opioids will be recorded. The obtained data will be compared statistically.

NCT ID: NCT04171544 Completed - Spinal Disease Clinical Trials

Streamline Occipito-Cervico-Thoracic System Post-Market Clinical Follow-up

OCT PMCF
Start date: August 6, 2019
Phase:
Study type: Observational

This is a multi-center, post-market, retrospective study design to collect safety and performance data for patients implanted with the Streamline OCT System.

NCT ID: NCT04166981 Completed - Spinal Stenosis Clinical Trials

Instr. vs. Non-instr. Posterolateral Spinal Fusion in Patients With Spinal Stenosis and Degenerative Listhesis

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

The aim of this study is to determine, in patients with grade 1 degenerative spondylolisthesis with spinal stenosis, if decompression and lumbar spinal fusion with, or without supplementary pedicle screw fixation yields an improved patient reported outcome.

NCT ID: NCT04094220 Completed - Clinical trials for Lumbar Spinal Stenosis

LLIF Plus Posterior Decompression for Severe Lumbar Spinal Stenosis

Start date: August 1, 2019
Phase: N/A
Study type: Interventional

Lateral lumbar interbody fusion (LLIF), as a minimally invasive technique, is an indirect decompression technique, and its decompression effect is not as thorough as traditional posterior decompression surgery. For certain patients with severe lumbar stenosis, additional posterior decompression is required. However, whether additional posterior decompression is necessary for these patients is unknown. Radiographic predictors of failed indirect decompression via LLIF is unknown. In current randomized, controlled trial , the investigators compare the clinical outcomes of patients with severe lumbar stenosis who received LLIF plus posterior decompression and those without posterior decompression.

NCT ID: NCT04087811 Completed - Clinical trials for Lumbar Spinal Stenosis

Postmarket Registry for Evaluation of the Superion® Spacer

PRESS
Start date: November 28, 2016
Phase:
Study type: Observational [Patient Registry]

To gather evidence documenting the performance and clinical outcomes associated with treatment of moderate degenerative lumbar spinal stenosis using the Superion® Indirect Decompression System (IDS).

NCT ID: NCT04087694 Completed - Clinical trials for Lumbar Spinal Stenosis

Microdecompression Versus Open Laminectomy and Posterior Stabilization for Multilevel Lumbar Spine Stenosis

Start date: January 3, 2016
Phase: N/A
Study type: Interventional

This study compare the results of 2 methods in surgical treatment of Lumbar spine stenosis.These are microdecompresssion and open decompression with posterior stabilization. 100 patients are involved in this study who divided in 2 groups.Each group was treated with one method and follow up done which showed both method are effective with better results in those patients treated with microdecomppression.

NCT ID: NCT04079894 Completed - Low Back Pain Clinical Trials

Physical Activity in the Elderly Spine Patient

PAESP
Start date: June 26, 2019
Phase:
Study type: Observational [Patient Registry]

Purpose Physical activity reduces the risk of several diseases of the body and the mind1, 2 and can help the elderly maintain physical abilities and self-efficacy in daily life1. The overall purpose of the project is to provide clinicians with a tool to objectively assess physical activity in daily life and thus provide an informed basis for individualized care of elderly patients with spine disease. We would like to introduce this tool to a broad population of elderly patients with low back pain to give an overview of the range and variability in physical activity. We will also look into a method for accurate step count in spine disorders where patients have severe walking impairment due to affected lumbar nerve roots.

NCT ID: NCT04062942 Completed - Clinical trials for Lumbar Spinal Stenosis

The Six-Minute Walking Test (6WT) and Timed-Up-and-Go (TUG) Test as Measures of Objective Functional Impairment in Patients Undergoing Interlaminar or Transforaminal Epidural Steroid Injection for Lumbar Degenerative Disc Disease (DDD)

Start date: July 15, 2019
Phase:
Study type: Observational

The primary objective is to determine the validity of the Six-Minute-Walking Test (6WT) and Timed-Up and Go (TUG) test to measure objective functional impairment (OFI) in patients undergoing either interlaminar epidural steroid injection (ESI) or transforaminal epidural steroid injections (TFESI) for lumbar degenerative disc disease (DDD)

NCT ID: NCT04062474 Completed - Spinal Stenosis Clinical Trials

Epidural Intervention of Spinal Nerves With Tumor Necrosis Factor-Alpha Inhibitor

Start date: May 15, 2016
Phase: N/A
Study type: Interventional

This study is to assess the clinical efficacy of epidural injections with Tumor Necrosis Factor-Alpha(TNF-α) Inhibitor in patients with chronic radicular pain caused by lumbar spinal stenosis.

NCT ID: NCT04058171 Completed - Low Back Pain Clinical Trials

Validation of a Treadmill Walking Test to Discriminate Neurogenic Claudication From Vascular Claudication

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

The first aim of this study was to elaborate and validate a treadmill walking test that would help discriminate between neurogenic claudication from vascular claudication. The second objective of this study is to determine if the treadmill walking test can discriminate spinal stenosis from low back pain with radiating pain in lower limb.