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Spondylolisthesis clinical trials

View clinical trials related to Spondylolisthesis.

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NCT ID: NCT03945461 Completed - Spondylolisthesis Clinical Trials

Return of Bowel Function After One or Two Level Anterior Lumbar Interbody Fusion With Chewing Gum

Start date: February 13, 2019
Phase: N/A
Study type: Interventional

Researchers are trying to identify is chewing gum improves bowel function after anterior lumbar interbody fusion

NCT ID: NCT03928041 Completed - Clinical trials for Spondylolisthesis, Grade 1

A Clinical Study to Evaluate Safety and Performance of PEEK-OPTIMA™ HA Enhanced Interbody Cages in the Lumbar Spine

Start date: June 27, 2019
Phase: N/A
Study type: Interventional

The purpose of this trial is to collect clinical outcomes including radiographic and CT outcomes in patients who undergo interbody spinal fusion using the EVOS Lumbar Interbody System.

NCT ID: NCT03898232 Completed - Clinical trials for Degenerative Disc Disease

Fibergraft Interbody Fusion Retrospective

FIFR
Start date: May 9, 2019
Phase:
Study type: Observational

A single center study of clinical and radiological outcomes in a retrospective cohort of patients treated with Lumbar Interbody Fusion augmented with Prosidyan Fibergraft for 1 or 2 level degenerative spinal disease by a single surgeon. Study Design: Retrospective chart review with prospective data collection.

NCT ID: NCT03884283 Completed - Clinical trials for Degenerative Disc Disease

Prospective, Multi-center Study to Assess Posterolateral Fusion Using FIBERGRAFT

Start date: February 19, 2019
Phase: N/A
Study type: Interventional

This is a prospective, non-randomized (single arm), multi-center, post-market clinical study designed to evaluate FIBERGRAFT® BG Matrix mixed with autograft and bone marrow aspirate in up to 150 subjects with degenerative disc disease (DDD) with or without radiculopathy, or spinal stenosis and/or spondylolisthesis requiring a fusion. The patient population will include adult (skeletally mature) men and women undergoing 1 or 2 level fusion in the lumbar spine (L2-S1) who are deemed eligible for the study, characterized by inclusion and exclusion criteria.

NCT ID: NCT03746418 Completed - Clinical trials for Lumbar Fixation Surgery

Effect of Addition of Dexmedetomidine During Ultrasound Guided Bilateral Single Shot Erector Spinae Plane Block in Patients Undergoing Posterior Lumbar Interbody Fusion Under General Anesthesia

Start date: January 1, 2016
Phase: Early Phase 1
Study type: Interventional

Posterior lumbar interbody fusion (PLIF) is the management of choice in double level lumbar (L) spondylolisthesis (L3-L5) after ineffective conservative treatment. We evaluated bilateral ultrasound (US)-guided single shot erector spinae plane (ESP) block at the level of lumbar 3 (L3) vertebra with or without dexmedetomidine (Dex).

NCT ID: NCT03647501 Completed - Clinical trials for Lumbar Spinal Stenosis

Lumbar Fusion With Nexxt Spine 3D-Printed Titanium Interbody Cages

Start date: August 22, 2018
Phase: N/A
Study type: Interventional

The purpose of this randomized controlled trial is to assess and compare radiographic and clinical outcomes in patients who are to undergo combined interbody/posterolateral lumbar fusion procedures, supplemented with pedicle screw instrumentation, using one of the following interbody cages; the Nexxt Spine Nexxt MatrixxTM 3D-printed titanium cage or the HonourTM poly-ether-ether-ketone cage.

NCT ID: NCT03585439 Completed - Clinical trials for Surgical Procedure, Unspecified

Isthmic Spondylolisthesis Treated With Combined Approach: Clinical and Radiological Outcomes

SPLAC
Start date: June 28, 2018
Phase:
Study type: Observational

This study aims to evaluate clinical and radiological outcomes of isthmic spondylolisthesis surgically treated with combined approach. The goal is to demonstrate that it is a safe and efficient technique to treat isthmic spondylolisthesis. There is very little literature concerning this procedure.

NCT ID: NCT03459404 Completed - Postoperative Pain Clinical Trials

Sufentanil NanoTab PCA System/15 mcg for Acute Post-Operative Pain in Vertebral Surgery: A Preliminary Investigation

Start date: September 19, 2018
Phase:
Study type: Observational

The Zalviso® Sufentanil Sublingual Tablet System (SSTS) (Grünenthal Italia, Milan, Italy) is a patient-controlled analgesia (PCA) system approved in September 2015 by the European Commission for the management of acute moderate-to-severe pain in adult patients in a hospital setting. This preprogrammed drug/device combination product delivers a fixed dose of 15 mcg of sufentanil tablets as needed, in a non-invasive sublingual dosage form. Multimodal analgesia is defined as the administration, by one or more routes, of various analgesic medications with different mechanisms of action, thereby providing superior analgesia with fewer side effects. To improve pain control and patient satisfaction, patient-controlled analgesia (PCA) techniques have been developed, i.e. any delivery system which allows patients to self administer predetermined doses of analgesic drug to relieve pain. Over the past decades, intravenous (IV) PCA with morphine has been the gold standard for acute pain control. In our clinical practice, though, not only IV-PCA pumps were frequently prone to technical problems, but also patients and caregivers were not often able to understand or activate them, thus raising important safety issues and profoundly affecting the management of pain control. As a consequence, IV-PCA eventually fell into disuse, although no alternative has emerged until recently. The SSTS should go beyond the above-quoted limitations: it is a non invasive, patient-controlled and easy to use device, with an effective and safe opioid profile. It is, in our thinking, a promising technology. The aim of this retrospective analysis is to examine the role of the SSTS for management of pain after vertebral surgery, as part of a multimodal approach.

NCT ID: NCT03425682 Completed - Clinical trials for Degenerative Disc Disease

ViBone in Cervical and Lumbar Spine Fusion

Start date: May 14, 2018
Phase:
Study type: Observational

Assess clinical and radiographic outcomes in patients who undergo 1-3 level anterior cervical discectomy fusion (ACDF) or lumbar interbody fusion (TLIF, PLIF, ALIF, or LLIF) using ViBone.

NCT ID: NCT03327298 Completed - Clinical trials for Lumbar Spondylolisthesis

Free Hand Lumbar Pedicular Screw Fixation

Start date: May 10, 2014
Phase: N/A
Study type: Interventional

Background: Different methods for lumbar pedicular screw insertion have been advocated, however each technique has its cons and pros. Due to limited resources for O-Arm and navigation in our locality, the investigator was enforced to use the surgical skills to minimize the need for such advanced modalities. Aim of the study: Is to clarify the benefits of the use of free hand technique using direct visualization of the pedicles and disc space as the only guide for pedicular screw insertion using postoperative CT for evaluation of the accuracy of pedicle screw insertion. Patients and methods: One hundred and forty four screws were inserted in 32 patients using direct pedicle visualization and disc space orientation as a single intraoperative reference guide. The study was conducted in Zagazig University Hospitals from May, 2014 to June, 2015. CT was done for all patients as a direct postoperative evaluation tool.