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Spine Surgery clinical trials

View clinical trials related to Spine Surgery.

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NCT ID: NCT03112993 Completed - Spine Surgery Clinical Trials

Speed of Recovery of Reversal of Neuromuscular Blockade in Geriatric Patients Undergoing Spine Surgery

Start date: May 30, 2017
Phase: Phase 4
Study type: Interventional

Spine surgery is one of the most common operative procedures in the United States. It is performed in the prone position (a patient laying on belly). Muscle relaxants are given for neuromuscular blockade often referred as paralysis for surgical exposure which is maintained until the patient is returned to the supine position (a patient laying on back) at the end of surgery. At the end of the surgery the paralysis is reversed with a drug (neostigmine). A new drug (sugammadex) has the ability to rapidly reverse the paralysis but it is not well investigated in elderly. This study will investigate speed of recovery and complications of the two reversal drugs in elderly patients (age ≥ 65 years) undergoing posterior spine surgery.

NCT ID: NCT02949518 Completed - Clinical trials for Enhanced Recovery After Surgery

Enhanced Recovery After Spine Surgery

Start date: November 28, 2016
Phase: N/A
Study type: Interventional

Enhanced recovery pathways (ERP) after surgery have been shown to decrease length of stay and perioperative complications in a range of surgical specialties. To date, ERPs has not been studied in patients presenting for spine surgery. The investigators have recently developed an interdisciplinary pathway for spine surgery patients based on the latest available evidence and guidelines. The aim of this trial is to compare the investigators enhanced recovery pathway with conventional perioperative management in patients undergoing 1-2 level posterior lumbar fusion.

NCT ID: NCT02884440 Completed - Low Back Pain Clinical Trials

Transverse Abdominis Plane Block for Anterior Approach Spine Surgery

TAP ALIF
Start date: November 7, 2016
Phase: Phase 2
Study type: Interventional

Therapeutic, prospective, randomized, double blind, placebo-controlled, in intention to treat, monocentric study to evaluate the analgesic efficacy of a bilateral TAP block after spine surgery with 24 hours morphine consumption

NCT ID: NCT02606695 Completed - Spine Surgery Clinical Trials

Comprehensive Spinal Alignment Planning Study

Start date: March 2016
Phase:
Study type: Observational

A comprehensive approach to the evaluation of alignment in spinal surgery patients - through preoperative planning, intraoperative assessment, and postoperative confirmation - has not been well-studied. This study aims to assess the value of such planning through clinical and radiographic outcomes.

NCT ID: NCT02162368 Completed - Airway Management Clinical Trials

Laryngeal Mask Use in Knee-chest Position in Lumbar Surgery in Neurosurgical Patients

Start date: January 2008
Phase: N/A
Study type: Observational

Spine surgery is the most common procedure in neurosurgical setting. Some centers have chosen the patient self-position to avoid complications such as accidental extubation or loss of the iv line. The aim of our retrospective study is to describe our experience in the laryngeal mask use for airway management in patient submitted to spine surgery in neurosurgery

NCT ID: NCT00967109 Completed - Anemia Clinical Trials

Establishment of Optimal Transfusion Threshold During Spine Surgery

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

The purpose of this study is to determine whether a higher threshold for transfusion with red blood cells improves the tissue oxygenation.

NCT ID: NCT00840996 Completed - Spine Surgery Clinical Trials

Perioperative Intravenous Lidocaine or Epidural Anesthesia on Outcomes in Complex Spine Surgery

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

The purpose of this study is determine if epidural anesthesia administered after surgery or lidocaine administered during surgery will decrease inflammation after spinal surgery and decrease the need for post operative pain medication compared to intravenous patient controlled analgesia. Participants undergoing spine surgery will be randomized into one of two groups; - A.) General Anesthesia and postoperative Patient Controlled Analgesia and placebo IV infusion. B.) General Anesthesia plus perioperative intravenous lidocaine infusion, and post operative Patient Controlled Analgesia.

NCT ID: NCT00618592 Completed - Spine Surgery Clinical Trials

Does Pre-operative Carbohydrate Loading Reduce Insulin Resistance and Improve Outcomes in Elective Surgical Patients?

Preop
Start date: February 2008
Phase: N/A
Study type: Interventional

The recent development of an oral carbohydrate drink for consumption prior to elective surgical procedures has been shown to improve insulin sensitivity. However, these studies have not investigated the use of this carbohydrate supplement in patients undergoing cardiac and spinal surgery. Hypothesis: The administration of 100g of carbohydrates the evening before and 50g of carbohydrates two hours before elective coronary artery bypass graft (CABG) or spinal surgery will reduce postoperative insulin resistance by 40% compared to those undergoing the standard of care of fasting the evening before and the day of surgery.

NCT ID: NCT00494832 Completed - Spine Surgery Clinical Trials

Influence of Dexmedetomidine on the Evoked Potentials During Spine Surgery

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

The purposes of this study are: 1. To evaluate the safety and efficacy of Dexmedetomidine as an adjunct for anesthesia during spine surgery and 2. To investigate the influence of Dexmedetomidine on the evoked potentials.

NCT ID: NCT00459966 Completed - Spine Surgery Clinical Trials

Preoperative Prevention and Early Rehabilitation for Patients Undergoing Elective Spine Surgery

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

Aim: The aim is to evaluate the outcome after spine surgery when using an integrated program that combined preoperative prevention and early postoperative rehabilitation compared to the routine procedures. Outcome measurements: Postoperative hospital stay, complications, function, pain, and patient satisfaction. Method: 60 patients scheduled for surgery for degenerative lumbar disease. The control group followed the routines in the department. The intervention group followed the integrated program consisting of preoperative prevention.