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Scoliosis clinical trials

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NCT ID: NCT01663909 Completed - Pain Clinical Trials

Pain Management Using Guided Imagery for Adolescents Post-spinal Fusion

Start date: May 2010
Phase: N/A
Study type: Interventional

Surgery to correct scoliosis (spinal fusion)generates a severe pain intensity rending pain management a complex task. Several studies have found out that pharmacological interventions alone were not enough to provide optimal pain management for these patients. The investigators developed a DVD on guided imagery, customized for teenagers, to help them cope better with their pain. The investigators believe that this type of intervention combined with their usual analgesic medication will help them to control their pain and foster rehabilitation.

NCT ID: NCT01661998 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

Prospective Study of Motion Preservation Evaluation Below Fusions of the Spine in Adolescent Idiopathic Scoliosis

POM
Start date: June 2008
Phase:
Study type: Observational

The purpose of this study is to evaluate the relationship of A) The distal fusion level B) The total length of fusion and the post-operative range of motion in the unfused vertebral segments below the fusion in patients with Adolescent Idiopathic Scoliosis.

NCT ID: NCT01661959 Enrolling by invitation - Clinical trials for Adolescent Idiopathic Scoliosis

Adolescent Idiopathic Scoliosis Outcomes Database Registry

AIS
Start date: January 2005
Phase:
Study type: Observational

The purpose of this study is to analyze the long-term outcomes of surgical treatment of idiopathic scoliosis of all curve patterns treated by either anterior or posterior procedures. In addition, to analyze the long-term outcomes of non-operative idiopathic scoliosis.

NCT ID: NCT01633931 Active, not recruiting - Clinical trials for Adolescent Idiopathic Scoliosis

Treatment of Adolescent Idiopathic Scoliosis Patients Using the Ellipse MAGEC System

Start date: March 2012
Phase: N/A
Study type: Observational

The purpose of this study is to collect data on the use of the Ellipse MAGEC System to treat patients with adolescent idiopathic scoliosis (AIS) who have failed external brace therapy.

NCT ID: NCT01610908 Completed - Scoliosis Clinical Trials

Multicenter Schroth Exercise Trial for Scoliosis

MultiSETS
Start date: April 2011
Phase: N/A
Study type: Interventional

The primary aim of this multicenter randomized controlled trial is to compare the effect of a 6 month "Schroth exercise program combined with standard-of-care" to "standard-of-care alone" on scoliosis curve severity measured using the Cobb angle. Secondary aims include: 1. To determine the effect of Schroth exercises at 6 months on secondary outcomes including quality-of-life, spinal appearance, objective posture and spinal muscle endurance measurements. 2. To determine the efficacy of 6 months of Schroth therapy offered to control participants after completing 6 months in the standard-of care group (using subjects as their own controls) 3. To determine if the effects of the 6 months supervised Schroth exercise program can be maintained after supervised therapy is terminated. At Hopital Ste-Justine, the following secondary aims will be pursued to examine the preliminary evidence about the effect of Global Postural Re-education (to satisfy the local ethics committee request because Global Postural Re-education exercises were offered routinely to patients at that institution prior to the trial). A. To compare the effect and to quantify the treatment effect sizes of 6 months of "Global Postural Re-education exercises with North American standard Care consisting of only observation and bracing" to "Schroth exercises combined with North American standard care" and to "North American standard care alone" on scoliosis curve severity measured using the Cobb angle. B. To estimate the effect and quantify the treatment effect sizes of 6 months of "Global Postural Re-education exercises with North American standard Care" to "Schroth exercises combined with North American standard care" and to "North American standard care alone" on outcomes including quality-of-life, perceived spinal appearance, objective posture and spinal muscle endurance measurements. C. To determine if the effects of "Global Postural Re-education exercises with North American standard Care" can be maintained after discontinuing supervision. D. To estimate the feasibility of conducting a randomized trial focused on Global Postural Re-education exercises by quantifying enrollment rates, attendance at scheduled exercise sessions and compliance with the home exercises prescribed.

NCT ID: NCT01588054 Completed - Scoliosis Clinical Trials

Prospective Radiographic and Clinical Evaluation of Surgical Treatment for Cervical Deformity

PCD
Start date: January 9, 2013
Phase:
Study type: Observational

The purpose of this study is to define clinical and demographic features within the population suffering from cervical deformity to assist health professionals to make important treatment decisions.

NCT ID: NCT01581021 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

Pedicle Screw Usage in Conventional Fixation Pattern Constructs Compared to Thoracic Hook Constructs in Scoliosis

Start date: August 2005
Phase: N/A
Study type: Interventional

Scoliosis is a deformity in which there is an abnormal curvature of the spine. Surgery is the main method of correcting this deformity. Rods are attached to the spine to make it strait. There are two ways to fix these rods to the bone of the spine: laminar hooks or pedicle screws. Hooks are an older form of fixation and do not penetrate the bone, but are instead placed over a part of the vertebra called the lamina. Screws are newer and do penetrate the bone. Screws are placed into the part of the vertebra called the pedicle. Most surgeons think screws correct scoliosis better than hooks. The current literature agrees that screws are better for deformity correction in the lumbar spine and patients with severe deformity. There is disagreement in the literature regarding which works better in the thoracic spine in less severe deformity. There are no randomized, controlled trials in the literature that examine whether constructs that use hooks in the thoracic spine and screws in the lumbar spine (called hybrid constructs) work as well as all-screw constructs. This clinical study is a randomized controlled trial being conducted to evaluate treatment outcomes in patients with scoliosis undergoing surgical correction for their curves using either all-screw or hybrid constructs as fixation devices. The study population is limited to those with less severe deformity and the investigators' hypothesis is that hybrid constructs will be as acceptable as screws in terms of correction.

NCT ID: NCT01570491 Completed - Scoliosis Clinical Trials

A Real-Time Ultrasound Guided Approach For Spinal Anesthesia

Start date: March 2012
Phase: N/A
Study type: Interventional

Our goal was to compare the number of attempts to perform spinal anesthesia using real-time ultrasound guidance versus landmark technique in patients meeting predefined criteria for difficult spinal anesthesia.

NCT ID: NCT01550497 Completed - Low Back Pain Clinical Trials

Spinal Stabilization Exercises for Low Back Pain in Adolescents With Idiopathic Scoliosis

LBPAIS
Start date: March 1, 2012
Phase: N/A
Study type: Interventional

1. Do spinal stabilization exercises demonstrate immediate and long-term effects of weight weeks of spinal stabilization exercises as measured by pain intensity and quality of life scores? 2. Does eight weeks of spinal stabilization exercises improve back muscle endurance in adolescents with Idiopathic Scoliosis (IS) with low back pain (LBP), compared to a one-time treatment (control)? Hypotheses: The research hypothesis for Question 1 is: Participants who receive eight weeks of spinal stabilization exercises will demonstrate significantly improved pain intensity and quality of life scores compared to participants who receive a one-time treatment after eight weeks of the intervention period and at six-month follow-up. The research hypothesis for Question 2 is: Participants who receive eight weeks of the spinal stabilization exercises will demonstrate significantly improved back muscle endurance, compared to participants who receive a one-time treatment after eight weeks of intervention.

NCT ID: NCT01549873 Completed - Clinical trials for Idiopathic Scoliosis

Anesthesia During Neurophysiologic Monitoring in Scoliosis Patients

Start date: January 2012
Phase: N/A
Study type: Interventional

When patients have spinal surgery, electrodes are placed on the body to measure motor evoked potentials (MEP) and somatosensory evoked potentials (SSEP). Many hospitals only use IV anesthesia because they feel that measuring MEP and SSEP is easier using IV anesthesia. At this hospital the investigators typically use inhaled anesthesia and are able to successfully measure MEP and SSEP. This is a study to find out if one method of anesthesia is better than the other for measuring MEP and SSEP.