Clinical Trials Logo

Clinical Trial Summary

Significant pain may occur following posterior spinal fusion despite the use of conventionally accepted techniques including patient controlled analgesia. If detected, a significant reduction in opioid requirements may lead to improved patient satisfaction and decreased opiate side effects.

The current study would use a prospective, randomized trial investigating the efficacy of one of 2 regimens as adjuncts to intraoperative anesthesia and postoperative analgesia, along with a third control group. The patients would be randomized to receive remifentanil plus a single intraoperative dose of methadone; remifentanil plus a bolus followed by an infusion of magnesium; or remifentanil alone. In addition, the two medications being studied might make it easier to determine the efficacy of neurophysiologic monitoring including somatosensory evoked potential (SSEP) (amplitude and latency) and motor evoked potential (MEP) (mA) required to elicit the response.

The purpose of this study would be to explore the effects of intraoperative methadone vs magnesium on intraoperative anesthetic requirements, postoperative opioid requirements, the efficacy of neurophysiologic monitoring including SSEP and MEP, inspired concentration of desflurane, remifentanil, and the need for intraoperative supplemental agents to control blood pressure.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01795495
Study type Interventional
Source Nationwide Children's Hospital
Contact
Status Completed
Phase Phase 2
Start date September 2013
Completion date September 2016

See also
  Status Clinical Trial Phase
Recruiting NCT04539522 - Efficacy of a Three-dimensionally Corrective Exercise Therapy for Scoliosis N/A
Recruiting NCT05128279 - Adolescent and Young Adulte Scoliosis
Withdrawn NCT04633031 - The Effect of Bracing on Sagittal Balance in Scoliosis
Recruiting NCT03978273 - Effects of Real-Time Feedback Assisted Self-Correction on the Posture of Scoliotic Patients N/A
Recruiting NCT06161038 - Precision Medicine for Nociception, Sngception and Proprioception. N/A
Not yet recruiting NCT06055140 - Evaluation of Thoracolumbar Fascia and Relationship With Low Back Pain in Individuals With Idiopathic Scoliosis
Active, not recruiting NCT05001568 - Validation of a New Optimized Nighttime Providence Brace for Personalized Treatment of Adolescent Idiopathic Scoliosis N/A
Terminated NCT03663088 - Effect of Global Postural Re-education in Idiopathic Scoliosis N/A
Recruiting NCT05575596 - Influence of Social Deprivation and Remoteness on Quality of Life in Adolescent's Surgical Scoliosis
Completed NCT04714632 - Function of Inner Ear Such as Balance and Perception of Verticality in Children With Idiopathic Scoliosis
Not yet recruiting NCT05347056 - The Effect of Vertebral Body Tethering on Lumbar Paraspinal Muscle Cross-Section Area in Adolescent Idiopathic Scoliosis
Completed NCT05333796 - The Effect of Back Muscles Activation on Idiopathic Scoliosis Using Surface Electromyography N/A
Completed NCT03190668 - Skeletal Muscle and Adipose Tissue Study Phase 4
Completed NCT03209752 - Prediction of 3D Effect of Brace in Idiopathic Scoliosis Treatment Using EOS Imaging System and "Anatomic Transfer".
Active, not recruiting NCT02651324 - Efficacy of Ketamine for Improvement in Postoperative Pain Control After Spinal Fusion for Idiopathic Scoliosis Phase 4
Completed NCT01019109 - Scoliosis Surgery Using the PASS® LP System
Not yet recruiting NCT06298812 - REFLECT Scoliosis System Post Approval Study N/A
Recruiting NCT06331143 - Analgesic Efficacy of Mid-Transverse Process to Pleura (MTP) Block and Intrathecal Morphine in Idiopathic Scoliosis Patients Undergoing Posterior Spinal Fusion N/A
Completed NCT05095129 - The Role of Genetic Factors in the Development of Idiopathic Scoliosis in the Kazakh Population
Completed NCT02199314 - Anesthesia and Motor Evoked Potential (MEP) Recruitment N/A