Clinical Trials Logo

Scoliosis clinical trials

View clinical trials related to Scoliosis.

Filter by:

NCT ID: NCT04069637 Completed - Clinical trials for Early-Onset Scoliosis Deformity of Spine

Serum and Urine Titanium Levels in Children With Early Onset Scoliosis Treated With Growth-Sparing Instrumentation

Start date: November 7, 2019
Phase:
Study type: Observational [Patient Registry]

The investigators are conducting research to compare serum and urine titanium levels in children with early onset scoliosis who are being treated with certain types of metal spinal rods. These rods include traditional growing rods (TGR), magnetically-controlled growing rods (MCGR), and Vertical Expandable Prosthetic Titanium Rib (VEPTR). Children with metal rods may have elevated serum and urine titanium levels. These levels may remain elevated over time. The investigators will collect serum titanium levels from children with metal rods and children without metal rods to see if there are differences in their titanium levels. The investigators will then collect a second serum titanium level from children with metal rods at least 6 months later to see if the participants titanium levels remain elevated over time. The investigators will also collect urine titanium levels from children with metal rods to see if titanium is excreted in the urine.

NCT ID: NCT04069169 Completed - Clinical trials for Scoliosis; Adolescence

IV Lidocaine Analgesia in Pediatric Scoliosis Surgery

P-IVLT
Start date: December 18, 2019
Phase: Phase 3
Study type: Interventional

Surgical correction of scoliosis in children is a long procedure, with an equivalently long recovery time, that is commonly performed at BC Children's Hospital. Treating pain immediately after the procedure is a priority for children during recovery. Morphine is one medication that can be used to manage post-operative pain, but unfortunately, its use is accompanied by a number of side effects which can affect recovery. These include nausea, vomiting, pruritus, sedation, dysphoria, respiratory depression, constipation, ileus, and urinary retention. In order to control pain and reduce morphine consumption, intravenous lidocaine is being investigated. This therapy has been beneficial in adult populations undergoing abdominal surgery and has been associated with decreased post-operative pain, decrease use of opioids including morphine, and ileus. These all contribute to shorter lengths of stay in the hospital and better recovery in the adult population. Intravenous lidocaine is used by some anesthesiologists at BC Children's Hospital to manage post-operative pain in children receiving surgical correction for scoliosis, but this is not a standard of practice. We now propose to conduct a double-blind randomized controlled trial to determine if intravenous lidocaine, infused from start of anesthesia up to 48 hours post-operatively, will reduce morphine use and improve post-operative pain in the pediatric population.

NCT ID: NCT04063670 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

Coping After Pediatric Scoliosis Surgery

CAPS
Start date: May 1, 2019
Phase: N/A
Study type: Interventional

This is a prospective, randomized controlled trial evaluating the efficacy of expanded patient education and coping skills on pain management following multilevel pediatric spinal surgery. The intervention will include a smartphone- based platform and a comprehensive library of peri-operative educational and coping skills videos as a means for better addressing the psychosocial elements of a child's individual pain experience. The study evaluated whether this novel intervention will reduce pain, improve outcomes and accelerate functional recovery up to 6 weeks after surgery.

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: 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: 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: 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

NCT ID: NCT03968146 Completed - Clinical trials for Scoliosis Idiopathic

Erector Spinae Plane Block in Scoliotic Adolescents

Start date: June 18, 2019
Phase: Phase 2
Study type: Interventional

For scoliotic surgeries, Erector Spinae Plane Block (ESPB) can add to the multimodal approach for perioperative pain management with decreasing the opioids requirement, improving recovery and decreasing ICU stay.

NCT ID: NCT03894865 Completed - Scoliosis Clinical Trials

Screening and Prevalence of Adolescent Idiopathic Scoliosis in Selected Urban and Countryside Schools in Egypt

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

Early detection of scoliosis and determination of which areas are more affected urban or countryside will help in early management. Also, this will guide the government and the community for early intervention to decrease the factors that leads to this postural abnormality. This also will guide another clinician to search for the cause of these posture deformities and to concentrate screening for special areas with special cultures.