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Spinal Cord Diseases clinical trials

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NCT ID: NCT06242054 Completed - Clinical trials for Cervical Spine Myelopathy

Motor Function Assessment System Based on Video Tracking and Artificial Intelligence Technique

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to develop a motion recognition system based on video tracking technology and combine it with artificial intelligence technology to form a motion recognition and function evaluation system in in healthy people and patients with cervical spondylotic myelopathy. The main questions it aims to answer are: - The development of this motion recognition system, - In the scenario of hand motor dysfunction, the key parameters of hand movement in healthy people and patients with cervical spondylotic myelopathy were evaluated, and the hand motor function model was established to achieve an objective, highly sensitive, highly specific, repeatable and easy-to-use system in clinical hand motor function evaluation. Participants will recieved the evaluation of this system and mJOA before the surgery. If there is a comparison group: Researchers will compare the evaluation results of healthy people to see if this system could recognized the hand motor dysfunction of patients with cervical spondylotic myelopathy.

NCT ID: NCT05994404 Completed - Clinical trials for Cervical Spondylosis With Myelopathy

Cervical Spondylotic Myelopathy - Cost Observational Surgical Trial

CSM-COST
Start date: April 1, 2014
Phase:
Study type: Observational

The purpose of the study is to determine the cost-effectiveness of different surgical strategies to treat cervical spondylotic myelopathy. The study will use data generated from the CSM-S Trial (NCT02076113). 1. To determine if laminoplasty is more cost-effective compared to dorsal fusion or ventral fusion surgery. 2. To determine the relative cost-effectiveness between anterior cervical discectomy and fusion (ACDF), posterior instrumented cervical fusion (PCF), and cervical laminoplasty.

NCT ID: NCT05927662 Completed - Clinical trials for Displacement of Intervertebral Disc Without Myelopathy

Results of Mini-open Discectomy According to Sagittal Profile

Start date: February 1, 2019
Phase:
Study type: Observational

In the normal healthy population, the sagittal alignment can be divided into four types based on the size of the sacral slope and lumbar lordosis. The effect of this sagittal profile especially type 2 with almost straight lordosis on the clinical outcomes of patients after mini-open discectomy is unknown. In this study, the results of patients who underwent mini-open discectomy were evaluated according to sagittal profile types of the patients.

NCT ID: NCT05659121 Completed - Stroke Clinical Trials

Improving Mobility Via Robotic Exoskeletons in Local Rehabilitation Settings in Singapore

Start date: November 15, 2018
Phase: N/A
Study type: Interventional

The programme is designed to investigate the application of robotic exoskeleton in different levels of local rehabilitation facilities. Feasibilities, efficacy, cost-effectiveness, patient and therapist's view of the application of robotic exoskeleton will be evaluated.

NCT ID: NCT05240612 Completed - Clinical trials for HTLV-1-Associated Myelopathy (HAM)

A Clinical Pharmacological Study of MT-3921 in Subjects With HTLV-1 Associated Myelopathy (HAM)

Start date: May 2, 2022
Phase: Phase 1
Study type: Interventional

The purposes of this study is to assess the safety, tolerability, and pharmacokinetics of MT-3921 in subjects with Human T-cell Leukemia Virus Type 1 (HTLV-1)-Associated Myelopathy(HAM). Subjects meeting eligibility criteria will enter the 6-month double-blind period. Subjects will be randomized in a 2:1 ratio to receive MT-3921 or placebo in a double blind manner.

NCT ID: NCT05003219 Completed - Cervical Myelopathy Clinical Trials

Long Term Clinical Outcome of Single Open Door Laminoplasty With Preservation of Unilateral Muscular Ligament Complex

Start date: August 1, 2019
Phase:
Study type: Observational

To collect and measure the preoperative and postoperative clinical data of the patients undergoing single open-door expansive laminoplasty with preservation of musclar ligament complex through posterior cervical approach in our hospital and summarize the long-term clinical effect and postoperative imaging changes and analyze the long-term clinical effect of this operation

NCT ID: NCT05001685 Completed - Cervical Myelopathy Clinical Trials

Study on the Postoperative Complications and Changes in Posterior Cervical Muscle Volume After Cervical Single Open-door Expansive Laminoplasty With Preservation of Muscular Ligament Complex

Start date: August 1, 2019
Phase:
Study type: Observational

In 2006, our hospital improved and began to use cervical expansive open-door laminoplasty preserving the unilateral ligament with muscle complex.The effect of recent follow-up, postoperative complications and their effects on posterior cervical muscle volume were also studied.However, there are few reports about medium and long-term follow-up.

NCT ID: NCT04968054 Completed - Clinical trials for Cervical Spondylotic Myelopathy

Comparison of IONM Between Remimazolam and Propofol

Start date: July 20, 2021
Phase: N/A
Study type: Interventional

Inhalation anesthetics significantly can delay latency and reduce amplitude of cortical MEPs and SSEPs signals compared to intravenous anesthetics by acting on not only GABA (γ-aminobutyric acid) receptors but also NMDA (N-methyl-D-aspartate) receptors, so total intravenous anesthesia (TIVA) have been more preferred for neurophysiological monitoring follow-up during surgery. However, just less than inhalation anesthetics, the decrease of amplitude and the delay of latency also occur according to the dose dependant of propofol. Moreover, it can cause various adverse effects such as delayed recovery after anesthesia or propofol infusion syndrome, consequently, combined methods with other agents or conversion to other relative anesthetics are being made. Remimazolam is a ultra-short-acting benzodiazepine, and unlike conventional benzodiazepine drugs, it is rapidly metabolized in plasma and not accumulates in the body for long periods of infusion or even with high dose administration. Recently, there have been repored that continuous infusion of 0.5-1.5 mg/kg of remimazolam has little effect on the motor evoked potential (MEPs) of cervical spine surgery patients, but this is a case report without the control group; further prospective studies are definitely needed. Therefore, in the case of using propofol or remimazolam for total intravenous anesthesia, we aim to investigate which intravenous anesthetic is more appropriate for intraoperative neurophysiological monitoring by comparing the results of the somatosensory evoked potential (SSEPs) and MEPs according to these anesthetics.

NCT ID: NCT04962256 Completed - Cervical Myelopathy Clinical Trials

ERAS in Posterior Approach of Cervical Spine Operation

Start date: March 20, 2019
Phase:
Study type: Observational

Enhanced recovery after surgery (ERAS) strategy has been used in the patient management of different diseases. This study aims to evaluate the effectiveness of ERAS in the perioperative period of posterior approach of cervical spine operation among patients with CSM.

NCT ID: NCT04947891 Completed - Cervical Myelopathy Clinical Trials

The Establishment of the Integration of Surgery and Postoperative Intensive Recovery of Patients With CSM

Start date: December 6, 2017
Phase:
Study type: Observational

This study aims to establish the specialist consensus of the integration of posterior approach surgical treatment and postoperative intensive recovery management for CSM or OPLL patients, and verify its safety, practicability and reliability.