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Scoliosis clinical trials

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NCT ID: NCT01089140 Terminated - Clinical trials for Non-idiopathic Scoliosis

Non-Idiopathic Scoliosis Treated With Tranexamic Acid

Start date: November 2014
Phase: Phase 2
Study type: Interventional

Investigation of tranexamic acid (TXA) for reducing perioperative blood loss and transfusion requirement in pediatric patients with secondary scoliosis undergoing posterior spinal fusion.

NCT ID: NCT01087034 Completed - Scoliosis Clinical Trials

Bracing During Infantile Scoliosis: Airways Study

MASI
Start date: February 2010
Phase: N/A
Study type: Observational

Idiopathic juvenile thoracic scoliosis is a tridimensional deformation of the spine which may impact on the intrathoracic organs. Bracing is one of the oldest treatments of spinal deformities. It relies on the indirect manipulation of spinal curvatures in order to prevent curve progression, which may affect respiratory function. The acoustic reflection method is based on the analysis of the reflection of a single transient planar wave giving the longitudinal cross-sectional area profile of the examined cavity. It is noninvasive and harmless. The EOS™ device allows a double incidence, full body, and low-dose X-ray acquisition with thoracic 3D reconstruction. The aim of the study is to evaluate the impact of bracing on the upper airways patency (by means of the acoustic method), on the breathing pattern (noninvasive respiratory muscles assessment), and on the thoracic penetration index (by means of the EOS™)

NCT ID: NCT01045473 Not yet recruiting - Spinal Stenosis Clinical Trials

Prospective Study of Minimally Invasive Spine Surgery

Start date: January 2010
Phase: N/A
Study type: Observational

The population of the US is aging. They remain more active and place greater demands on their musculoskeletal system. A key problem is that pain and disability of age related spinal disorders will increase. Problems such as Degenerative Lumbar Spondylolisthesis, Degenerative Disk Disease, Spinal Stenosis and Degenerative Scoliosis are age related problems that are treated with spinal fusion when non-operative treatment fails. Traditional open surgery poses significant risk for patients in this age group. The use of minimally invasive spinal surgery techniques provides an opportunity to treat these patients with less morbidity than traditional open surgery.

NCT ID: NCT01019109 Completed - Clinical trials for Idiopathic Scoliosis

Scoliosis Surgery Using the PASS® LP System

Start date: May 2010
Phase:
Study type: Observational

The purpose of this study is to find out the outcomes of using the PASS LP System to correct idiopathic scoliosis. This system is a unique set of spinal instrumentation used to surgically correct the rotation and deformity of the spine that is caused by scoliosis. Also, this study wants to find out the effects this system has on the physical appearance and quality of life for patients with scoliosis.

NCT ID: NCT00994656 Completed - Scoliosis Clinical Trials

Is Pleth Variability Index (PVI) a Surrogate for Pulse Pressure Variations (PPV) in Pediatric Spine Fusion (SF) Surgery?

Start date: October 2009
Phase: N/A
Study type: Observational

Spine fusion is an involved procedure during which patients are at risk for significant intra-operative blood loss.This study will compare 2 ways of determining fluid status and response to fluid administration. One way is to measure the changes in the arterial wave form from the special IV that is usually placed in an artery (PPV). The second way is to use a non-invasive method of a finger probe that measures changes in the plethysmogram or the pleth variability index (PVI). No actual patient treatments will be based on these values during surgery.

NCT ID: NCT00989495 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

Comprehensive Cohort Study of Bracing for Adolescent Idiopathic Scoliosis (AIS): A Feasibility Study

Start date: October 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to gain initial experience and information for proper planning and conduct of a confirmatory study (a multi-centre single-blind comprehensive cohort study of bracing).

NCT ID: NCT00958581 Completed - Scoliosis Clinical Trials

Tranexamic Acid (TXA) Versus Epsilon Aminocaproic Acid (EACA) Versus Placebo for Spine Surgery

Start date: December 2008
Phase: Phase 4
Study type: Interventional

Tranexamic acid (TXA) and epsilon aminocaproic acid (EACA) have been reported to reduce blood loss in the cardiac surgery literature but they have not been reported in use head-to-head in the orthopedic surgery literature. In a randomized, double-blind, prospective study we believe that TXA will be more effective than both EACA and placebo at reducing blood loss for corrective spinal surgery.

NCT ID: NCT00958542 Suspended - Cerebral Palsy Clinical Trials

Prospective Study of Cerebral Palsy Scoliosis

Start date: March 2009
Phase: N/A
Study type: Interventional

This is a prospective, multi-centre study that will be looking at two groups of males and females over the course of their operative treatment for cerebral palsy (CP) scoliosis and the years following that treatment. The first group the study will be looking at is those individuals who undergo surgery for CP Scoliosis. The second group will be those individuals who do not undergo surgical treatment for CP Scoliosis, either because the family declines surgery or surgery is not recommended during the course of study participation.

NCT ID: NCT00958373 Withdrawn - Clinical trials for Adolescent Idiopathic Scoliosis

Risk Factors for Psychiatric Disorders Associated With Adolescent Idiopathic Scoliosis

Start date: October 2006
Phase: N/A
Study type: Observational

The purpose of this pilot study is to determine the presence, frequency, and severity of mental health disorders amongst adolescents undergoing spinal surgery for scoliosis.

NCT ID: NCT00890227 Completed - Scoliosis Clinical Trials

Incidence of Proximal Junctional Kyphosis (PJK) in Long Posterior Spinal Fusion: A Study Comparing Traditional Open Surgery to Minimally Invasive Percutaneous Technique at the Proximal Fusion Levels

Start date: June 2009
Phase: N/A
Study type: Interventional

This research is being done to compare two methods of surgery to treat scoliosis and/or kyphosis of the spine.