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Scoliosis clinical trials

View clinical trials related to Scoliosis.

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NCT ID: NCT01336114 Completed - Scoliosis Clinical Trials

A New 3D Geometrical Modelisation of Adolescent Idiopathic Scoliosis and Conception of a Personal Brace

MODEL MAKER
Start date: July 2011
Phase: N/A
Study type: Observational

Adolescent idiopathic scoliosis (AIS) involves complex tridimensional deformities of the spine. In case of progressive curve deformity, the use of spinal bracing remains the standard non operative treatment of moderate AIS. Most of the time, the different types of braces don't take into account the individual biomechanical properties of each patient's spine. Actually, it is essential to better understand the effect of the loads applied on the trunk and on the spine, and a 3D geometrical modelisation of these components is essential. Many studies have been publishing concerning the use of radiographs for the geometrical reconstruction of the spine, and more recently the EOS system. But even then, it is still necessary to obtain an important number of geometrical data and discretisation is still a long procedure.

NCT ID: NCT01325493 Completed - Spondylolisthesis Clinical Trials

Low Dose Ketamine Study on Opioid Tolerance and Hyperalgesia

KPSF
Start date: January 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to: 1. Establish whether ketamine can decrease opioid consumption and modulate the onset of opioid tolerance and prevent opioid-induced hyperalgesia in pediatric subjects, ages 10 years to 18 years, undergoing posterior spinal fusion and instrumentation.

NCT ID: NCT01292252 Completed - Clinical trials for Lumbar Spondylolisthesis

Use of Forteo (Teriparatide) in Posterolateral Lumbar Spine Fusion

Start date: August 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effects of 12 weeks of daily treatment with teriparatide on spine fusion in adult patients who are undergoing multi-level posterolateral spine fusion surgery for degenerative conditions of the lumbar spine.

NCT ID: NCT01205256 Completed - Scoliosis Clinical Trials

IRB-HSR# 14145 R,S Methadone: Analgesia and Pharmacokinetics in Adolescents Undergoing Scoliosis Correction

Start date: March 2009
Phase: Phase 3
Study type: Interventional

This is a pilot study to determine the pharmacokinetics of (R,S) methadone in adolescents. A total of approximately 15 patients will be required. The purpose is to determine the levels of R, S methadone at various time intervals after drug administration. Patients will receive methadone 0.25 mg/kg IV at induction and a standardized anesthetic of remifentanil and propofol. At the conclusion of surgery (45 minutes prior to the completion), the patients will receive a loading dose of morphine based on respiratory rate. A morphine PCA will be utilized for postoperative analgesia. Pharmacokinetic data will be collected in addition to VAS scores, patient and parental satisfaction with analgesia, and a functional pain assessment.

NCT ID: NCT01163955 Completed - Scoliosis Clinical Trials

A Postural Study Comparing Sitting on the Floor Versus Sitting in a Chair While Playing Video Games.

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

To determine if sitting in a chair or sitting on the floor lends itself to better posture while playing video games.

NCT ID: NCT01148888 Completed - Scoliosis Clinical Trials

The Effect of Magnesium Sulfate on Motor and Somatosensory Evoked Potentials in Children Undergoing Scoliosis Surgery

Start date: June 2010
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to determine whether magnesium sulfate has a clinically important effect on the amplitude and latency of somatosensory and motor evoked potentials in patients undergoing surgical correction of idiopathic scoliosis.

NCT ID: NCT01135940 Recruiting - Wounds Clinical Trials

The Use of Dermabond Versus Standard Staple for Wound Closure in Children With Neuromuscular Scoliosis Undergoing Spinal Deformity Correction Surgery

Start date: May 2010
Phase: Phase 2
Study type: Interventional

This is a prospective, Phase II (hypothesis generating) randomized pilot study investigating the efficacy of using Dermabond as a method of final wound closure as compared to the standard staple method in children with Neuromuscular Scoliosis undergoing spinal deformity correction surgery.

NCT ID: NCT01109082 Completed - Scoliosis Clinical Trials

Gait and Postural Stability Assessment in Children With Idiopathic Scoliosis Undergoing Posterior Spine Instrumentation

Start date: December 2007
Phase: N/A
Study type: Observational

The goal of this study is to evaluate children and adolescents with idiopathic scoliosis who are undergoing spinal fusion using motion analysis, balance, and outcome questionnaires. Little research has been done to evaluate how different fusion levels impact walking patterns, range of motion, posture and balance following spine instrumentation in children with idiopathic scoliosis. Debate still continues whether posterior spinal instrumentation with the last instrumented vertebra at or above Lumbar 3 (L3) will provide sufficient spine correction, greater motion, and better posture and balance when compared to a child with instrumentation at Lumbar 4 (L4). Furthermore, how does the spine fusion endpoint (last instrumented vertebra) impact quality of life, participation, and impairment in children and adolescents with idiopathic scoliosis and how do they compare to healthy age-matched peers. The goal of this study is to compare these two end points using gait analysis, postural stability, and outcome tools with the hopes of providing better clinical care to children with idiopathic scoliosis.

NCT ID: NCT01108211 Completed - Scoliosis Clinical Trials

Improving Low Bone Mass With Vibration Therapy in Adolescent Idiopathic Scoliosis (AIS)

Start date: January 2009
Phase: Phase 3
Study type: Interventional

This is a prospective randomized controlled trial investigating the effect of vibration therapy on bone mineral density (BMD) and bone quality in AIS subjects suffering from osteopenia (low bone mass).

NCT ID: NCT01103115 Completed - Scoliosis Clinical Trials

Calcium + Vitamin D Supplementation for Low Bone Mass in Adolescent Idiopathic Scoliosis (AIS)

Start date: April 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether Calcium and Vit D supplementation is effective for improving low bone mass in Girls with Adolescent Idiopathic Scoliosis (AIS).