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Adolescent Idiopathic Scoliosis clinical trials

View clinical trials related to Adolescent Idiopathic Scoliosis.

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NCT ID: NCT04950660 Recruiting - Clinical trials for Adolescent Idiopathic Scoliosis

Oral Caffeine Use for Pain Management in AIS Patients After Spinal Fusion

Start date: December 11, 2019
Phase: Phase 4
Study type: Interventional

Prospective, randomized control trial To determine if oral caffeine decreases the frequency of opioid demand in children with adolescent idiopathic scoliosis after their spinal fusion surgery To compare pain scale ratings, number of requests for diazepam, average heart rate, average blood pressure, sex, age, ethnicity, post-op day of discharge, operative time, estimated intraoperative blood loss, remittance post-surgery, length of hospital stay, and segments fused during spinal fusion surgery.

NCT ID: NCT04931433 Completed - Analgesia Clinical Trials

Intravenous Lignocaine as an Analgesic Adjunct in Adolescent Idiopathic Scoliosis Surgery

IGNITE-AIS
Start date: December 24, 2020
Phase: Phase 4
Study type: Interventional

This is a single-center study comparing the effect of intravenous (IV) Lignocaine given throughout posterior spinal fusion surgery on the reduction of morphine usage during postoperative period in adolescent idiopathic scoliosis (AIS) patients.

NCT ID: NCT04929678 Active, not recruiting - Clinical trials for Adolescent Idiopathic Scoliosis

Study of the Braive Growth Modulation System for Progressive Pediatric Scoliosis

BRAIVE IDE
Start date: August 12, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to establish probable benefits and evaluate the safety and preliminary effectiveness of the Braiveā„¢ GMS when used in the treatment of pediatric progressive scoliosis.

NCT ID: NCT04921813 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

Investigation of Conservative Treatment on Adolescent Idiopathic Scoliosis Patients.

Start date: August 15, 2014
Phase: N/A
Study type: Interventional

Aim: It was aimed to investigate the effectiveness of three-dimensional scoliosis exercises and balance-coordination exercises in patients with adolescent idiopathic scoliosis.

NCT ID: NCT04889339 Not yet recruiting - Scoliosis Clinical Trials

Validation of a New Generation of Orthopedic Brace for Treating Adolescent Idiopathic Scoliosis by Using Growth Modulation

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

Adolescent Idiopathic Scoliosis affects 3-4% of the Canadian population, of which about 10% will need a brace treatment during pubertal growth spurt. Our team has developed an innovative conception method for brace design by simulating the growth modulation using numerical models. Those models are customized to each patient. In this project, the investigators will evaluate the effectiveness of this platform customized treatment and validate its clinical application.

NCT ID: NCT04877236 Withdrawn - Clinical trials for Adolescent Idiopathic Scoliosis

Green Sun Medical Dynamic Brace

Start date: November 21, 2019
Phase: N/A
Study type: Interventional

The Green Sun Medical Dynamic Brace (GSM) brace was developed as an alternative to rigid thoracolumbosacral orthoses (TLSOs, braces) commonly used to prevent continued curve progression in patients with adolescent idiopathic scoliosis (AIS). The brace applies corrective forces to the muscular and bony structures of the spine while preserving range of motion (ROM). The innovative design of this brace should provide an equivalent degree of correction of the scoliotic curvature as a rigid TLSO, with increased acceptability to the patient via improved comfort and spinal/chest wall mobility. Increased acceptability promotes increased adherence to treatment. This is a pilot study to collect preliminary short-term data concerning the safety and performance of the GSM brace in a sample of subjects with AIS who are currently being treated with a TLSO. The study will use clinical exams, x-rays, monitoring equipment, and questionnaires to primarily assess safety and performance. Secondary endpoints include spinal ROM and lung vital capacity assessment, as well as data validation. The study involves 3 visits, a performance check phone call, and 4 follow up calls over a four month span. This is a pilot study and no formal hypothesis testing will be done. Descriptive statistics of selected variables will be calculated.

NCT ID: NCT04868331 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

Cardiovascular Responses in Adolescent Idiopathic Scoliosis Girls

Start date: May 18, 2021
Phase: N/A
Study type: Interventional

The aims of this pilot study are to determine the metabolic demand and exercise intensity level of E-Fit exercise intervention by evaluating the cardiovascular responses in AIS girls and whether the cardiovascular responses for AIS girls performing E-Fit will behave in the same way as compared to healthy controls. We hypothesise that 1) the metabolic demand and exercise intensity of E-Fit exercise intervention is equivalent to moderate-to-vigorous level; and 2) AIS girls have different cardiovascular responses as compared to healthy controls

NCT ID: NCT04867148 Active, not recruiting - Clinical trials for Ankylosing Spondylitis

The Prediction and Prevention of Disease by Using Big Data in Motion Analysis

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

Variable patterns of gait disturbance can be found in patients with spine disease including the problems of gait initiation, freezing of gait, reduced balance and postural control, reduced step lengths, increased step times, and slow walking speed.

NCT ID: NCT04761549 Enrolling by invitation - Clinical trials for Adolescent Idiopathic Scoliosis

3D, Dynamic and Mechanically-informed Decision Making in AIS

3D-AIS
Start date: January 19, 2021
Phase: N/A
Study type: Interventional

Adolescent Idiopathic Scoliosis (AIS) is a growth defect of the spine that primarily occurs in prepubertal children between the age of 10 to 14 years, affecting approximately 3% of these otherwise normal children. AIS has been associated with problems related to posture, load-related back pain, as well as aesthetic problems, e.g. the induced asymmetry of the shoulder. Therefore, early diagnosis followed by the appropriate treatment is vital to prevent further curve progression of AIS and minimize the health-related complications of these patients. The current treatment recommendation to stop curve progression for an immature patient with a scoliosis curve between 25 and 40 degrees is to wear a brace. If the curve in the skeletally immature patient is not responding to the brace treatment, dynamic scoliosis correction by vertebral body tethering can be considered when there is still some growth potential left. State-of-the-art guidelines for the selection of fusion levels are currently mainly based on two-dimensional (2D) static radiographic parameters (such as, the Cobb angle and Shoulder balance) and a qualitative assessment of 2D bending or traction radiographs. Several classification systems and algorithms that are based on the 2D static radiographic (X-ray) parameters exist to assist surgeons in determining the appropriate levels to be instrumented. Despite this wide range of classification systems and detailed guidelines available in the literature, spinal fusion does not always yield satisfying 2D radiographic clinical outcome, with revision rates ranging from 3.9% to 22%. Overall, the surgeon is presently not provided with 3D dynamic and mechanical information regarding the deformity of the AIS to guide the decision-making. Obtaining this vital 3D dynamic information regarding the curvature and mechanical behavior of the spine will allow the surgeon to make an evidence-based and well-informed decisions in the treatment of the AIS patient. Consequently, realizing these objectives has the potential to improve patient satisfaction, reduce the postoperative complications and accordingly reduce socio-economic costs associated with AIS treatment. Recent advances in the use of subject specific musculoskeletal models will form the basis to realize this shift from 2D to 3D dynamic in AIS care.

NCT ID: NCT04760808 Recruiting - Clinical trials for Adolescent Idiopathic Scoliosis

Evaluation of Cerebrospinal Fluid Flow in Adolescent Idiopathic Scoliosis

MEDULLOSCOL
Start date: February 1, 2021
Phase:
Study type: Observational

Adolescent Idiopathic Scoliosis (AIS) is the most frequent spinal deformity in adolescence, but its etiology remains unknown. Recent publications suggest a link between ciliopathy and AIS. More specifically a modification of the cerebro-spinal fluid (CSF) flow by ciliary dysfunction could be at the origin of a scoliotic deformity. This study aims to compare the CSF flow measured by magnetic resonance imaging (MRI) in an AIS group and a control group.