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Scoliosis; Adolescence clinical trials

View clinical trials related to Scoliosis; Adolescence.

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NCT ID: NCT05326256 Completed - Clinical trials for Scoliosis Idiopathic

Trunk Proprioception in Adolescent Idiopathic Scoliosis

Start date: February 2, 2022
Phase: N/A
Study type: Interventional

Aims of this clinical research: - To investigate trunk proprioception in all three planes in individuals with adolescent idiopathic scoliosis (AIS), - To investigate the pelvis orientation sense in all three planes in individuals with adolescent idiopathic scoliosis, - To investigate whether trunk proprioception and pelvis orientation sense are improved with Physiotherapy Scoliosis Specific Exercises (PSSE) in AIS, - To investigate whether trunk proprioception and pelvis orientation sense are improved with vestibular exercise training to be added to PSSE exercises in AIS, - Comparison of the effects of different exercise training on trunk proprioception and pelvis orientation sense in AIS - To examine the parameters that may be associated with the improvement of trunk proprioception of different exercise training (health-related quality of life, perception of cosmetic deformity, scoliosis-related clinical features such as Cobb angle, axial trunk rotation, curve type, etc.).

NCT ID: NCT05325463 Completed - Clinical trials for Scoliosis; Adolescence

Lung Recruitment Maneuvers for Postoperative Atelectasis Prevention After Idiopathic Adolescents' Scoliosis Correction

Start date: April 10, 2022
Phase: N/A
Study type: Interventional

The investigators hypothesized that an ultrasound-guided lung recruitment maneuvers would be more effective in preventing postoperative atelectasis than conventional alveolar recruitment after surgical correction of idiopathic adolescent scoliosis.

NCT ID: NCT05259956 Completed - Clinical trials for Scoliosis; Adolescence

Trial on Two Treatments for Adolescent Idiopathic Scoliosis

Start date: February 18, 2022
Phase: N/A
Study type: Interventional

Adolescent Idiopathic scoliosis is a three-dimensional structural deformity of the spine and pelvic that occurs in children. More evidence has arisen to emphasize the important role played by pelvic asymmetry during the progression of scoliosis. The purpose of this study is to compare the effectiveness of pelvic adjustments accompanied with Schroth-based exercises, with the latter alone in adolescent idiopathic scoliosis, to assess the impact of pelvic asymmetry on the spinal three-dimensional parametric features in scoliosis.

NCT ID: NCT05227638 Completed - Clinical trials for Scoliosis; Adolescence

Investigation of the Efficacy of PNF and Schroth Treatment

Start date: November 10, 2021
Phase: N/A
Study type: Interventional

our study was to compare the advantages of Schroth and PNF methods used in AIS treatment

NCT ID: NCT05187780 Recruiting - Healthy Clinical Trials

Comparison of Reposition Sense in Scoliosis and Healthy Adolescents

Start date: January 22, 2022
Phase:
Study type: Observational

The aim of the study is to compare the spine joint reposition sense in adolescent idiopathic scoliosis and healthy adolescents and to investigate whether there is a difference.

NCT ID: NCT05185050 Completed - Clinical trials for Myofascial Pain Syndrome

Prevalence of Myofascial Pain Syndrome in Adolescent Idiopathic Scoliosis

Start date: October 10, 2021
Phase:
Study type: Observational [Patient Registry]

this is an observational and cross-sectional prevalence study. 10-18 years aged participants with adolescent idiopathic scoliosis were recruited in the study. Myofascial pain syndrome will be questioned to the participants. additionally, all participants will be evaluated using their findings for scoliosis and myofascial pain syndrome diagnostic criteria. Cobb angle, coronal balance, shoulder and pelvis asymmetry, sagittal spino-pelvic parameters of the spine (cervical lordosis, thoracic kyphosis, lumbar lordosis angles and sagittal vertical axis, sacral slop angle and pelvic incidence) will be measured.

NCT ID: NCT05145725 Recruiting - Clinical trials for Scoliosis; Adolescence

Instrumented POsterolateral Arthrodesis for Adolescent Idiopathic Scoliosis

APOSIA
Start date: March 18, 2021
Phase:
Study type: Observational

The study population concerns adolescent patients with idiopathic scoliosis which requires surgical management and who have a longer waiting period of 6 months. The aim of this study is to research the predictive factors of an improvement in the quality of life of adolescents who have had surgery.

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: NCT04922983 Recruiting - Clinical trials for Scoliosis Idiopathic

Incobotulinumtoxin A and Yoga-like Isometric Exercise in Adolescent Idiopathic Lumbar Scoliosis

Start date: July 1, 2021
Phase: Phase 2
Study type: Interventional

The study uses a yoga-like isometric posture and botulinum injections to reduce the curves in adolescent idiopathic lumbar scoliosis. Three previous studies show that the yoga pose is effective for reversing scoliotic curves; Botulinum toxin has been approved by the FDA for teenagers. However, no studies using the two of them together have been done until this one.

NCT ID: NCT04899297 Recruiting - Quality of Life Clinical Trials

Quality of Life in Parents of Adolescents With Spinal Deformities: Development of a New Questionnaire.

Start date: May 7, 2021
Phase:
Study type: Observational

This study aims to develop a new instrument capable of providing an efficient measure of the quality of life of parents of conservatively treated patients with spinal deformity. The development of a questionnaire in a Rasch environment and specifically developed for parents of conservatively treated patients will ensure greater sensitivity and specificity of the questionnaire.