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Scoliosis clinical trials

View clinical trials related to Scoliosis.

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NCT ID: NCT04420143 Completed - Clinical trials for Degenerative Disc Disease

MLX/XLX ACR Expandable Lumbar Interbody Implants

Start date: January 27, 2020
Phase:
Study type: Observational

The objective of this study is to evaluate the safety and performance of thoracic and/or lumbar spine surgery using the MLX and XLX ACR interbody implants as measured by reported complications, radiographic outcomes, and clinical patient outcomes. This study is being undertaken to identify possible residual risks and to clarify mid- to long-term clinical performance that may affect the benefit/risk ratios of the MLX and XLX ACR interbody implants.

NCT ID: NCT04418817 Completed - Clinical trials for Degenerative Disc Disease

Modulus in XLIF Study

Start date: March 22, 2020
Phase:
Study type: Observational

The primary objective of this study is to evaluate the safety and performance of the Modulus 3D-printed titanium interbody implant in patients undergoing thoracic and/or lumbar XLIF as measured by reported complications, radiographic outcomes, and patient-reported outcomes.

NCT ID: NCT04403152 Completed - Clinical trials for Scoliosis Idiopathic

Postoperative Rehabilitation or Mobilization After Scoliosis Surgery

Start date: February 5, 2017
Phase: N/A
Study type: Interventional

Scoliosis surgery is a major surgery associated with postoperative pain, loss of physical function and pulmonary dysfunction in adolescent idiopathic scoliosis patients (AIS).Despite the advanced, various medical treatment methods of pain applied in the postoperative period, the mean period of hospitalization is 5 to 7 days. The increasing health expenditures over the years have brought along the need for rehabilitation programs conducted in the early term. Although early mobilization has been accepted as a rule of thumb by spinal surgeons in preventing the performance loss and reducing the causes of morbidity in recent years, the investigators could not find any research on postoperative rehabilitation implemented on patients under the supervision of a physiotherapist, following scoliosis surgery. The aim of this study was to compare effect of five days of intensive postoperative rehabilitation and mobilization on length of hospitalization and outcome in patients having scoliosis surgery.

NCT ID: NCT04282408 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

Experimental Evaluation of Back Braces for the Treatment of Spinal Deformity Produced With 3D Printing Technology

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

The proposed investigation is a pilot study that involves pediatric patients affected by spinal deformity (Adolescent Idiopathic Scoliosis and Osteogenesis Imperfecta). The main goal is to evaluate the acceptability, the safety and the overall satisfaction of the patients wearing the back braces produced with an innovative methodology using 3D printers, compared to the current braces manufactured with a production model based on thermoforming, that has well-established clinical efficacy.

NCT ID: NCT04244760 Completed - Cerebral Palsy Clinical Trials

Pain Assessment in Children Undergoing Spine Surgery

Start date: January 2015
Phase: N/A
Study type: Interventional

Musculoskeletal (MSK) pain is one of the most common types of pain among children and adolescents. Recurring episodes of MSK pain conditions have a major impact on the daily lives. Children and adolescents with neuromuscular diseases are often unable to report the pain the patients experience because of intellectual and/or physical limitations. There is no reason to believe that pain is any less frequent or intense in these patients than in normally developing patients. Because of the elusive nature of pain in non-verbal children, therapeutic decisions are frequently based on vague proxy measures of pain and revert to a series of trials and errors. This project creates a unique opportunity to directly characterize and compare MSK and surgical pain subjectively in two different patient samples (verbal and non-verbal). The ultimate goal is to use this information to offer the highest quality of pain control in children with MSK conditions, and more specifically in children with limited communication skills unable to communicate their distress associated with the surgical procedural.

NCT ID: NCT04215497 Completed - Exercise Clinical Trials

Effect of PSSE on Spine Reposition Sensation in Scoliosis

PSSE
Start date: October 1, 2018
Phase: N/A
Study type: Interventional

The main aim of the investigator's study is to investigate the effect of Physiotherapeutic Scoliosis-Specific Exercises (PSSE) on spine joint reposition sense and also to investigate the effect of PSSE on vertebral rotation, pain, posture, body image and quality of life in Adolescent Idiopathic Scoliosis (AIS). Twenty-six patients with AIS will randomly allocated to two groups. 'Schroth' exercises will apply to the PSSE group for 8 weeks (16 sessions). The control group wiil teach basic elements. Patients' spinal pain (Visual Analogue Scale), posture parameters (PostureScreen Mobile, Posterior Trunk Asymmetry Index (POTSI) and Anterior Trunk Asymmetry Index (ATSI)), cosmetic perception (Walter Reed Visual Evaluation Scale (WRVAS)), joint reposition sensations (dual-inclinometer), quality of life (Pediatric Quality of Life Scale and SRS-22) will assess at the first session and at the end of 8 weeks.

NCT ID: NCT04203394 Completed - Clinical trials for Scoliosis Idiopathic

Comparison of the Effects of Controlled Schroth Exercise and Home Exercise Programs

Start date: August 18, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to compare the effects of Schroth 3D exercise method on home symmetry, trunk topography, scapula symmetry, pelvic symmetry, health related quality of life and cosmetic deformity perception in adolescents with idiopathic scoliosis

NCT ID: NCT04183049 Completed - Pain Clinical Trials

Improved Rehabilitation After Spinal Surgery in Adolescents

Start date: December 18, 2019
Phase:
Study type: Observational

Impact of the OFA technique on postoperative recovery from adolescent spine surgery and the incidence of chronic postoperative pain.

NCT ID: NCT04175145 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

Impact of Metal Density on Deformity Correction for Adolescent Idiopathic Scoliosis

Start date: January 2014
Phase:
Study type: Observational

A retrospective analysis to ascertain the correlation between metal density and deformity correction among individuals with adolescent idiopathic scoliosis.

NCT ID: NCT04092335 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

Evaluation of Adam's Forward Bend Test and Smartphone Application in Screening of Adolescent Idiopathic Scoliosis

Start date: October 1, 2018
Phase:
Study type: Observational

Scoliosis is a lateral curvature of the spine when the Cobb´s angle more than 10˚ on the frontal plane. Curve detection before skeletal maturation gives a good opportunity for early treatment or prevention of curve progression. Purpose of this study was to evaluate Adam's Forward Bend Test and Scoliometer HD in screening of Adolescent Idiopathic Scoliosis