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Spine Disease clinical trials

View clinical trials related to Spine Disease.

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NCT ID: NCT05589402 Recruiting - Stroke Clinical Trials

Temporary Inactivation of Strong Muscle Sensation to Improve Rehabilitation Interventions in SCI

Start date: June 4, 2019
Phase: Phase 1
Study type: Interventional

The investigators are conducting a research study to try to improve rehabilitation interventions for individuals with spinal cord injury (SCI). In this study, the aim is to determine if temporarily numbing non-paralyzed arm muscles with an over-the-counter numbing cream while exercising paralyzed muscles, can improve the strength, function, and sensation of paralyzed muscles after a spinal cord injury.

NCT ID: NCT05530798 Recruiting - Clinical trials for Spinal Cord Injuries

CEUS For Intraoperative Spinal Cord Injury

Start date: December 1, 2023
Phase: N/A
Study type: Interventional

Spinal cord injury following posterior decompression in patients suffering from chronic, cervicothoracic spinal cord compression is a known complication with multiple etiologies. Currently, intraoperative neuromonitoring (IONM) remains the gold standard for predicting and preventing post-operative deficits from these procedures. However, there is a paucity in the field of spine surgery for further, non-invasive biomarkers that can help detect and prognosticate the degree of spinal cord injury intraoperatively. Contrast enhanced ultrasound (CEUS) is a radiation free imaging modality that utilizes nanobubble technology to allow for visualization of the macro- and microvascular architecture of soft tissue structures. Despite being currently approved for the use in hepatology and cardiology, it has remained absent from the field of spinal cord injury. The study team aims to evaluate and quantify micro- and macrovascular changes that lead to areas of hyper-perfusion as well as areas of ischemia intraoperatively in patients that undergo elective cervicothoracic posterior decompression for chronic compression. In addition, the study team aims to assess the efficacy of CEUS in detecting microvascular changes that correlate with IONM changes and predicting degree and recovery of post-operative neurologic deficits from intraoperative spinal cord injury. The study team hypothesizes that following decompression, subjects will have detectable levels of microvascular changes causing areas of hypoperfusion and reperfusion injury. Second, the study team hypothesizes that these perfusion changes will correlate with intraoperative neuromonitoring changes and can predict and prognosticate the degree of post-operative neurologic injury.

NCT ID: NCT05473689 Recruiting - Clinical trials for Spinal Cord Injuries

Outcomes Post Treatment: Impact on Motor Impairment of Sleep Efficiency in SCI (OPTIMISE SCI Trial)

Start date: August 15, 2022
Phase: N/A
Study type: Interventional

This randomized clinical trial will compare three groups of individuals with cervical/thoracic, complete or incomplete spinal cord injury (SCI) that will undergo: (i) early CPAP therapy in the management of moderate-to-severe sleep-related breathing disorders (SRBDs) among adults at 6 weeks after SCI; (ii) delayed CPAP therapy in the management of moderate-to-severe SRBDs among adults at 22 weeks after SCI; and (iii) no treatment as they either have mild or no SRBD.

NCT ID: NCT05453955 Completed - Spine Disease Clinical Trials

Effect of Remimazolam on Motor Evoked Potential

Start date: August 1, 2022
Phase: N/A
Study type: Interventional

This study was planned to investigate the degree of effect of remimazolam on MEP compared to propofol when monitoring the motion-inducing potential (MEP).

NCT ID: NCT05166018 Completed - Surgery Clinical Trials

Optimization of a Tool for Predicting Postoperative Clinical Evolution After Lumbar Surgery

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

The objective of the study is the establishment, optimization and prospective evaluation of a digital predictive platform capable of providing for each lumbar spine operated patient a clinical predictive status: Patient green (success) orange (treatment failure ), red patient (complication) in order to optimize his medical care up to 6 months.

NCT ID: NCT04983576 Completed - Clinical trials for Surgery--Complications

Risk Factors for Mechanical Failure After Spinal Fusion : an Observational Study

RachideMDS
Start date: August 30, 2021
Phase:
Study type: Observational

The aim of this of study is to identify the incidence of mechanical failures after spinal fusion within one year of surgery and to assess the related risk factors.

NCT ID: NCT04956588 Completed - Spine Disease Clinical Trials

Evaluation of the Safety and Efficacy of Smart Orthopedic Minimally Invasive Surgical Systems for Spinal Surgery

Start date: September 1, 2017
Phase: Phase 3
Study type: Interventional

To evaluate the safety and effectiveness of the intelligent orthopedic minimally invasive surgery system developed by Shenzhen Xinjunte Intelligent Medical Equipment Co., Ltd. in spinal surgery.

NCT ID: NCT04927273 Completed - Spine Disease Clinical Trials

Availability of Spine Neuronavigation in Africa

Start date: January 24, 2021
Phase:
Study type: Observational [Patient Registry]

In this study, the availability of spine neuronavigation in Africa was evaluated. Access to surgical equipment is an important goal of global surgery and global neurosurgery. The study findings show that there are regional differences in access to spine neuronavigation techniques and highlight that the major barriers to increased prevalence are cost and lack of trained personnel.

NCT ID: NCT04877470 Completed - Spinal Disease Clinical Trials

Baseline-characteristics of Patients Referred to a Secondary Spine Centre

CHAPARS
Start date: February 24, 2021
Phase:
Study type: Observational

A retrospective cohort study will be conducted in Zuyderland Medical Centre Heerlen, the Netherlands. All patients that were referred to the spine-centre between 01.01.2019 and 31.12.2019 will be included for analysis. This study aims to evaluate baseline characteristics, including baseline questionnaires, and information about the given treatments for all patients referred to the spine centre.

NCT ID: NCT04834141 Completed - Balance Clinical Trials

Correlation Between Thoracic Kyphosis Posture and Static Balance

Start date: October 13, 2020
Phase:
Study type: Observational [Patient Registry]

The effects of balanced posture and postural changes have been evaluated in specific populations with different factors that can affect body postures and balance, such as age, musculoskeletal system, and other metabolic diseases. Studies on postural kyphosis and balance involvement are very few in the literature especially in the health population. Of the few studies that have evaluated kyphosis and balance, most are limited by small sample size and the exclusion of men. Many have focused primarily on the geriatric population. The determination that the effect of thoracic kyphosis posture on trunk biomechanical alignment may be related to balance may contribute to new treatment recommendations in this area. The aim of this study is to investigate whether the thoracic kyphosis posture has an effect on static balance.