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Scoliosis clinical trials

View clinical trials related to Scoliosis.

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NCT ID: NCT05039255 Not yet recruiting - Clinical trials for Scoliosis Idiopathic

Acute Effects of Self-correcting Movement on the Balance and Spine of Patients With Scoliosis.

Start date: October 11, 2021
Phase:
Study type: Observational

The purpose of this study is to evaluate the acute effects of the self-elongation movement on the balance of patients (aged 8-16 years) suffering from adolescent idiopathic scoliosis,

NCT ID: NCT05033171 Completed - Clinical trials for Scoliosis Idiopathic

Rod Shape Changing After Scoliosis Correction Surgery

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

The change of the fixation-rod after posterior srew-rod fixation segmentdesis is not widely known. The recent development of the 3D scanning technics and the opportunities of the EOS 2D/3D system made us possible to have the exact rod shape immediately after implantation, and at each control examination. These progressions made us available to follow up the shape changing of the fixation-rod, hereby the changing of the correction.

NCT ID: NCT05011734 Recruiting - Clinical trials for Scoliosis Idiopathic

Rapid Postoperative Recovery Pathway in Adolescent Idiopathic Scoliosis.

Start date: November 3, 2021
Phase:
Study type: Observational

the study will evaluate the clinical outcomes of an intra- and postoperative fast-track protocol in patients undergoing instrumented posterior arthrodesis surgery for adolescent idiopathic scoliosis.

NCT ID: NCT05001568 Active, not recruiting - Scoliosis Clinical Trials

Validation of a New Optimized Nighttime Providence Brace for Personalized Treatment of Adolescent Idiopathic Scoliosis

Start date: November 15, 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 optimizing for the immediate in-brace correction. The model is customized to each patient. In this project, the investigators will evaluate the effectiveness of this platform's customized treatment and validate its clinical application.

NCT ID: NCT04992845 Terminated - Clinical trials for Adolescent Idiopathic Scoliosis

Fusionless Treatment of Idiopathic Scoliosis With the SCOLI-TETHER System During The Growth Period

FUTURE
Start date: April 15, 2019
Phase: N/A
Study type: Interventional

The goal of the study is to establish the safety and benefit of treatment of juvenile and adolescent idiopathic scoliosis (AIS) with the SCOLI-TETHER (MIScoli) System.

NCT ID: NCT04969770 Active, not recruiting - Clinical trials for Neuromuscular Scoliosis

Contribution of Muscle and Disc Elastography in the Evaluation of Biomechanical Modifications of the Neuromuscular Spine Fixed by Bipolar Construct

ELASTO
Start date: January 11, 2022
Phase: N/A
Study type: Interventional

Neuromuscular scoliosis are caused by a disorder of the brain, spinal cord or muscular system and often progressive at early age. Conservative treatment is not sufficient to maintain trunk and pelvic balance, and surgical treatment is frequently required. Early definitive spine fusion has the disadvantage of cessation of trunk growth with concomitant effects on lung development. Growth preserving spine surgeries are increasingly used but with high complication rates. The orthopaedic team at Necker Hospital Enfants maladies, Paris, France has developed an innovative fusionless surgery based on a bipolar spine construct, performed by a minimally invasive approach. The first 100 patients operated on with this technique had an average follow-up of 6.5 years. No arthrodesis, initially planned in adolescence, was necessary thanks to the stability of the correction of the deformities even after skeletal maturation. The main objective of the study was to analyze the progressive spinal stiffening, using muscle and disc elastography, in neuromuscular patients instrumented with this bipolar construct.

NCT ID: NCT04960423 Recruiting - Clinical trials for Degenerative Scoliosis

Clinical Study of Imaging and Endoplant-related Mechanical Complications After Long Segment Fixation and Fusion of Degenerative Lumbar Scoliosis (DLS)

Start date: January 1, 2020
Phase:
Study type: Observational

There is a high probability of mechanical complications in patients with degenerative lumbar scoliosis after long segment fixation and fusion, and there are few studies on distal borderline kyphosis deformity/failure. This study was designed to retrospectively analyze the patients with degenerative lumbar scoliosis (DLS) who underwent posterior selective decompression and long segment fixation and fusion surgery in the lumbar spine department of our hospital from April 2009 to May 2016. Patients' basic data, surgical data and preoperative, immediate postoperative and follow-up imaging data were collected to study the incidence of distal mechanical complications, risk factors and their relationship with clinical symptom scores in DLS patients undergoing posterior selective decompression and long segment fixation and fusion. It has guiding significance for clinical operation decision making.

NCT ID: NCT04959591 Completed - Clinical trials for Scoliosis; Adolescence

Use of Intravenous Acetaminophen in Pediatrics Undergoing Spinal Fusion Surgery

Start date: June 1, 2021
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate whether perioperative intravenous acetaminophen administration reduces postoperative pain and opioid consumption in adolescents and pediatric patients undergoing spinal fusion surgery.

NCT ID: NCT04952285 Completed - Tranexamic Acid Clinical Trials

The Efficacy and Safety of the Loading Dose of Tranexamic Acid in Scoliosis Surgery During Perioperative

Start date: January 1, 2015
Phase:
Study type: Observational

This study intends to make full use of the advantage of spinal orthopedic surgery in our medical center.Analyze the blood loss and blood coagulation function and the influence of safety of load dose tranexamic acid (TXA) in scoliosis surgery during perioperative.

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.