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Scoliosis clinical trials

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NCT ID: NCT00671931 Completed - Scoliosis Clinical Trials

Susceptibility of Motor-Evoked Potentials to Varying Targeted Blood Levels of Dexmedetomidine

Start date: April 2007
Phase: Phase 1
Study type: Interventional

Reduction of the spinal cord injuries during scoliosis surgery is a major goal of the anesthesia and surgical team. Despite improvement in scoliosis surgery over the years, the development of neurological deficits remains the most feared complication of spine surgery. During scoliosis surgery it is very important to monitor the spinal cord to detect spinal cord injury with surgical manipulation. Continuous or intermittent intraoperative electrophysiological monitoring (neuron-monitoring) is used routinely during these procedures to provide the surgeon with information concerning the integrity of neurological structures at risk. All neuron-monitoring modalities are affected by the anesthetic regimen used. Of the various intravenous anesthetic drugs, the combination of propofol, remifentanil and dexmedetomidine appear to impact neuron-monitoring the least. The current anesthetic practice is to use the three drugs in combination at doses that do not depress the signals but there is no data relating targeted dexmedetomidine and propofol blood levels to neuron-monitoring signals. The lack of data results in wide variability in dosing with consequent variability in patient response. Hypothesis: Clinically relevant blood levels of dexmedetomidine will affect the amplitude of transcranial motor-evoked potentials (TcMEP) either independently or by interaction with propofol in a dose dependent manner.

NCT ID: NCT00577226 Terminated - Scoliosis Clinical Trials

Shilla Growth Permitting Spinal Instrumentation System for Treatment of Scoliosis in the Immature Spine

Start date: April 2005
Phase: N/A
Study type: Observational

The objective of this study is to retrospectively and prospectively review patients who have undergone this technique looking at age of the patient, magnitude of the curve preoperatively, postoperatively and over time, diagnosis, pulmonary function, surgical procedures, complications, and spinal growth. The hypothesis is that Shilla growth permitting spinal instrumentation coupled with a surgical technique of aggressive correction of the apex of the scoliotic curve wil allow for natural growth of the spine in a guided fashion with a limited number of future surgeries required.

NCT ID: NCT00510575 Completed - Scoliosis Clinical Trials

Surgical Outcomes Using Variable Rod Diameters in the Treatment of Idiopathic Scoliosis

Start date: May 2007
Phase: Phase 4
Study type: Interventional

There are two rod sizes routinely used for the correction of juvenile and adolescent idiopathic scoliosis, 5.5mm and 6.35mm, typically stainless steel. Currently there is no scientific evidence supporting the superiority of one size rod relative to the other. This study will evaluate the amount of radiographic correction obtained using the 5.5mm versus the 6.35mm spinal instrumentation rods.

NCT ID: NCT00508066 Completed - Scoliosis Clinical Trials

Continuous Local Infusion of Anesthetic at the Incisional Site for Scoliosis Surgery

Start date: May 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the effects of continuous local anesthetic delivery on the immediate post-op recovery of patients undergoing spinal fusion surgery for congenital or idiopathic scoliosis.

NCT ID: NCT00448448 Terminated - Clinical trials for Adolescent Idiopathic Scoliosis

Bracing in Adolescent Idiopathic Scoliosis Trial (BrAIST)

BrAIST
Start date: February 2007
Phase: N/A
Study type: Interventional

Adolescent idiopathic scoliosis (AIS) is a structural curve of the spine with no clear underlying cause. Bracing is currently the standard of care for preventing curve progression and treating AIS. However, the effectiveness of bracing remains unclear. The purpose of this study is to compare the risk of curve progression in adolescents with AIS who wear a brace versus those who do not and to determine whether there are reliable factors that can predict the usefulness of bracing for a particular individual with AIS.

NCT ID: NCT00445393 Completed - Scoliosis Clinical Trials

Adolescent Idiopathic Scoliosis and Mental Health

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: NCT00411060 Recruiting - Osteoarthritis Clinical Trials

Clinical Orthopaedic Data Bank (Acute and Chronic)

Start date: January 2007
Phase:
Study type: Observational

Data involving orthopaedic conditions and rehabilitation aspects of musculoskeletal and neuromuscular disorders will be collected and stored as part of the normal clinical care of patients seen in the University of Florida (UF) and Shands Orthopaedics and Sports Medicine Institute.

NCT ID: NCT00323752 Completed - Scoliosis Clinical Trials

Recombinant Human Erythropoietin Compared to Autologous Pre-Donation Prior to Scoliosis Surgery in Children.

Start date: October 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to establish whether rHuEpo is as effective as PAD in increasing red cell mass prior to surgery. Other benefits of the PAD program and preoperative administration of rHuEpo will also be compared.

NCT ID: NCT00320619 Completed - Scoliosis Clinical Trials

Epsilon-Aminocaproaic Acid to Reduce the Need for Blood Transfusions During and Following Spine Surgery

Start date: September 2000
Phase: N/A
Study type: Interventional

Individuals who undergo spine surgery often have a significant loss of blood and may require multiple blood transfusions. Research has shown that epsilon-aminocaproic acid (EACA) may reduce the amount of blood lost during surgery, which would decrease the number of blood transfusions required. This study will evaluate the safety and effectiveness of EACA at reducing blood loss and the need for blood transfusions in individuals undergoing spine surgery.

NCT ID: NCT00273598 Completed - Scoliosis Clinical Trials

Comparing Two Instrumentation Systems for the Treatment of Adolescent Scoliosis

Start date: September 1997
Phase: Phase 2
Study type: Interventional

Idiopathic scoliosis affects 2-5% of adolescents. This study will compare the quality of life, functional outcome, cosmetic result, and the correction of spinal deformity of two instrumentation systems for the treatment of adolescent idiopathic scoliosis.