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Scoliosis clinical trials

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NCT ID: NCT04058561 Recruiting - Clinical trials for Early-Onset Scoliosis Deformity of Spine

Hospital-Based Cluster Trial: Magnetically Controlled Growing Rods Using Distraction Intervals

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

A hospital-based cluster stratified randomization control study will be conducted to investigate spinal growth in Early Onset Scoliosis patients between 5 and 9 years of age. Patients must have a major coronal curve measuring over 50 degrees and be undergoing Magnetically Controlled Growing Rod treatment. We will be studying 6-week lengthening intervals compared to 16-week lengthening intervals on spinal growth within 3 years.

NCT ID: NCT04047225 Recruiting - Clinical trials for Scoliosis Idiopathic

POSTOPERATIVE OPIOID-SPARING EFFECT OF INTRAOPERATIVE PAIN MONITORING USING THE ANALGESIA NOCICEPTIVE INDEX (ANI) DURING IDIOPATHIC SCOLIOSIS CORRECTION IN CHILDREN.

OpiSpANI
Start date: October 26, 2020
Phase: N/A
Study type: Interventional

Anaesthesia is often performed using a balanced technique by administering both opioids and anaesthetics agents. Intraoperative opioid administration is still relying on simple parameters such as heart rate and blood pressure variations. However, many studies in both adults and children have shown the poor accuracy of those parameters in predicting pain because of their sensibility to other intraoperative events such as depth of anaesthesia and volaemic variations. Consequently, intraoperative analgesia is still inadequately managed with periods of under dosage or over dosage of opioid agents. This has been hypothesized to cause postoperative hyperalgesia related to both intraoperative pain (in case of under dosage) or to opioid agents (in case of over dosage). The main resulting effect is an increase of postoperative opioid consumption and the inadequate postoperative rehabilitation because of adverse effects of opioids. During the last decade, many pain-monitors have been investigated. Most of these devices are relying on the determination of the sympathetic-to the parasympathetic systems balance. Among those monitors, the Analgesia Nociceptive Index (ANI) quantifies the parasympathetic system. The ANI device can produce two parameters the instantaneous ANI (ANIi), derived from 60 seconds analysis and the mean ANI (ANIm) derived from 4 minutes analysis. Studies have shown the accuracy of ANIi to detect both experimental and clinical pain in various populations. Moreover, a recent randomized controlled trial during spine surgery in adults has found ANIi to decrease the intraoperative and postoperative opioid consumption when used intraoperatively for guiding the administration of opioid agents

NCT ID: NCT04038229 Completed - Surgery Clinical Trials

Multidisciplinary Perioperative Care Pathway in Adolescents Undergoing Posterior Spinal Fusion Surgery

Start date: December 9, 2019
Phase: N/A
Study type: Interventional

Posterior Spinal fusion (PSF) is one of the most invasive orthopedic surgical procedures in children and adolescents, often characterized by extensive tissue trauma, and severe postoperative pain. In addition to pain, the postoperative period is complicated by the side effects of opioids such as nausea and vomiting, itching and sedation. Various studies have shown that pain in the direct postoperative phase is an important determinant for development of chronic post-surgical pain. The consequences of untreated acute pain are known and can also contribute to chronification in pain.

NCT ID: NCT04031716 Enrolling by invitation - Pain, Postoperative Clinical Trials

Comprehensive Study of Post-surgical Pain After Pectus or Spine Surgery

Start date: July 6, 2018
Phase: N/A
Study type: Interventional

This will be a prospective study to determine the association between specific genotypes, epigenetics, behavioral, social and biological factors, with the phenotypes, defined by pain perception, postoperative pain, analgesic effects, side effects to perioperative analgesics, chronic postoperative pain, and gene expression in patients following pectus excavatum repair.

NCT ID: NCT04021784 Completed - Clinical trials for Neuromuscular Scoliosis

Limited-efficacy Testing of SDS and NEMOST for Early Onset Neuromuscular Scoliosis

BiPOWR
Start date: May 6, 2019
Phase: N/A
Study type: Interventional

The primary aim of this study is to investigate and describe the limited efficacy of the Spring Distraction System (SDS) and Bilateral One Way Rod (NEMOST) in maintaining curve reduction without repeat lengthening procedures and complications. Secondary aims are to describe growth of the instrumented spine, health-related quality of life, and to compare both devices.

NCT ID: NCT04012528 Active, not recruiting - Scoliosis Clinical Trials

ERAS and Pediatric Scoliosis Surgery

RAAC
Start date: January 1, 2018
Phase:
Study type: Observational

The aim of this study is to compare the outcomes after scoliosis surgery before and after ERAS (enhanced recovery after surgery) program inplementation in children and teenager.

NCT ID: NCT04012125 Completed - Cerebral Palsy Clinical Trials

The Effect of Flexible Thoracolumbar Brace on Scoliosis in Cerebral Palsy

Start date: September 3, 2018
Phase: N/A
Study type: Interventional

The Effect of Flexible Thoracolumbar Brace on Scoliosis in Cerebral Palsy, Prospective, Randomized, Open-label Trial

NCT ID: NCT04012112 Completed - Clinical trials for Neuromuscular Scoliosis

The Effect of Flexible Thoracolumbar Brace on Spinal Alignment, Pain and Quality of Life in Subjects With Neuromuscular Scoliosis

Start date: August 23, 2018
Phase: N/A
Study type: Interventional

In the initial evaluation, the degree of spine is measured quantitatively using Cobb's angle and Muscular Dystrophy Spine Questionnaire (MDSQ). The patients who had Cobbs angle of 20-45 'by spinal plain radiography were evaluated for the effects of flexpine brace wearing and rehabilitation for 6 months. After 12 months, whole spine X-ray was taken for the followed up the patient's status.

NCT ID: NCT04003233 Withdrawn - Clinical trials for Idiopathic Scoliosis

Limited-efficacy Testing of Spring Distraction System (SDS) and Unilateral One-way Rod (MID-C) for Early Onset Scoliosis

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

The primary aim of this study is to investigate the limited efficacy of these innovative surgical solutions in treatment of Early Onset Scoliosis (EOS) in terms of maintaining reduction while maintaining spinal growth. The secondary aim is to compare both devices for these and other parameters as well as safety.

NCT ID: NCT03990376 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

Adolescent Idiopathic Scoliosis (AIS) Gold Standard for Blood Loss

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

The purpose of this study is to establish a benchmark for measuring blood loss by directly measuring the change in red cell volume before and after surgery and to compare established blood loss estimators to this benchmark in order to determine the most accurate and precise method for estimating blood loss in adolescent idiopathic scoliosis surgery patients