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Spinal Deformity clinical trials

View clinical trials related to Spinal Deformity.

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NCT ID: NCT06190873 Recruiting - Spinal Deformity Clinical Trials

The Effect of Telephone Education on Fear of Movement and Quality of Life in Patients With Lumbar Disc Herniation Surgery.

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

The aim is to quantify the fear of movement and quality of life of telephone education on lumbar disc herniation surgery.

NCT ID: NCT05856370 Recruiting - Spinal Deformity Clinical Trials

The Ailliance Post-Market Clinical Study

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

The purpose of this clinical study is to collect performance and safety data for post-market Medtronic devices indicated for cranial and/or spinal indication(s). Subjects are enrolled and followed postoperatively for up to 24 months. The Ailliance clinical study is intended to collect data congruous with routine clinical care practices.

NCT ID: NCT05714007 Recruiting - Surgery Clinical Trials

The Effects of Ferric Derisomaltose on Postoperative Anemia in Spinal Deformity Surgery

Start date: August 31, 2023
Phase: Phase 4
Study type: Interventional

The prognosis of patients undergoing spinal deformity surgery is often compromised by perioperative anemia due to iron deficiency. The aim of this randomized, controlled trial was to evaluate whether postoperative ferric derisomaltose intravenous injection may improve anemia and prognosis in patients undergoing spinal deformity surgery comparing with oral iron. Participants will be randomly assigned to the treatment group (intravenous ferric derisomaltose) and the control group (oral iron). Changes in hemoglobin concentration, percentage of anemia correction, changes in iron indicators, patient quality of life, and incidence of adverse events will be analyzed to evaluate the efficacy and safety of iron isomaltoside infusion.

NCT ID: NCT05648474 Recruiting - Spondylolisthesis Clinical Trials

Intraoperative Monitoring for the Lateral Lumbar Interbody Fusion Procedure

Start date: July 13, 2022
Phase:
Study type: Observational

This study is designed to evaluate the clinical utility of a known intraoperative neuromonitoring modality (SSEP) using saphenous nerve as the site of stimulation to identify changes to the lumbar nerves which may be at risk during the lateral lumbar interbody fusion (LLIF) procedure.

NCT ID: NCT05452057 Recruiting - Spinal Deformity Clinical Trials

Prehab for Adult Spinal Deformity Surgery

Start date: March 24, 2022
Phase: N/A
Study type: Interventional

Prehabilitation is defined as the process of enhancing patients' functional capacity and overall fitness to enable them to withstand a forthcoming stressor (e.g. surgery). Although there are different models of prehabilitation, multimodal prehabilitation is recommended to address the physical and psychological health outcomes prior to surgery. Multimodal prehabilitation commonly consists of exercise-training, nutritional, and psychological support. Evidence suggests that prehabilitation improves preoperative physical fitness and reduces postoperative complications and length of stay in patients undergoing major abdominal surgery. However, the evidence for the feasibility and effects in spinal deformity surgery are less understood. This study is a two arm, pilot randomized controlled trial to assess the feasibility of a multimodal prehabilitation program prior to surgery for spinal deformity in adults. Participant outcomes will be measured using standardized fitness testing, self-report questionnaires, and medical record reviews at baseline, one week preoperatively, and at 30 days postoperatively.

NCT ID: NCT05433545 Recruiting - Spinal Deformity Clinical Trials

Adherence to Physiotherapy Scoliosis Specific Exercises in Adolescents With Spine Deformity: Development of a New Questionnaire

Start date: March 22, 2022
Phase:
Study type: Observational

This study aims to develop a new instrument capable of providing an efficient measure of the quality and quantity of adherence to Physiotherapy Scoliosis Specific Exercises performed at home by growing patients with spinal deformity undergoing conservative treatment at a specialized institution. The development of a questionnaire in a Rasch environment and specifically developed for this population will ensure greater sensitivity and specificity of the questionnaire.

NCT ID: NCT05323448 Recruiting - Spinal Fusion Clinical Trials

Efficacy of ARISTA-AH for Restoring Hemostasis Following Posterior Long-segment Spinal Fusion.

Start date: October 25, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to assess the efficacy of the ARISTA AH for restoring hemostasis following a long segment posterior spinal fusion.

NCT ID: NCT05170815 Recruiting - Spinal Deformity Clinical Trials

Clariance ErYs Registry

ErYs
Start date: January 17, 2022
Phase:
Study type: Observational

International, prospective, single arm, multicenter and observational Post-Market Clinical Follow-up (PMCF). The overall objective of this study is to collect preoperative, intraoperative and postoperative (at 9 weeks, 6 months, 1 year and 2 years) data on the clinical complications and functional outcomes of the study devices to demonstrate safety and performance in a real-world setting. The primary objective is to demonstrate that the use of the study devices is safe. The secondary objective is to demonstrate that the use of the study devices decreases the pain, and improves the quality of life and the daily activities of the subjects.

NCT ID: NCT05146193 Recruiting - Spinal Deformity Clinical Trials

AI-Powered Scoliosis Auto-Analysis System Multicenter Development and Validations

Start date: May 1, 2022
Phase:
Study type: Observational

The investigators aim to use artificial intelligence (AI) to help clinicians in diagnosing and assessing spinal deformities.

NCT ID: NCT05108948 Recruiting - Spinal Deformity Clinical Trials

Research of Factors Determining the Improvement of Quality of Life at One Year of Adult Patients Treated for Spinal Deformity (COFTASD)

COFTASD
Start date: October 23, 2021
Phase:
Study type: Observational

The objective of this study is to find the predictive factors of improvement of the quality of life of operated patients from spinal deformity.