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Postoperative Complications clinical trials

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NCT ID: NCT03182062 Recruiting - Thoraric Surgery Clinical Trials

Individualized Perioperative Open-Lung Ventilatory Strategy During One-Lung Ventilation

iPROVE-OLV
Start date: September 8, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether individualized ventilatory management during one-lung ventilation in patients scheduled for thoracic surgery, combining the use of low tidal volumes, alveolar recruitment maneuvers, individually titrated positive end-expiratory pressure and individually indicated ventilatory support will decrease postoperative pulmonary complications, ICU and hospital length of stay compared to a standardized Lung Protective Ventilation (LPV).

NCT ID: NCT03181620 Recruiting - Postoperative Pain Clinical Trials

Sedation Administration Timing: Intermittent Dosing Reduces Time to Extubation

SATIRE
Start date: September 8, 2016
Phase: N/A
Study type: Interventional

SATIRE is a prospective, randomized control trial assessing two methods of administration of intravenous sedation and narcotics in surgical patients requiring mechanical ventilation. Many hospitals use a continuous infusion method of administering these medications. The investigators hypothesize that intermittent, bolus/sliding-scale based administration will lead to less medication being given and subsequently decrease the amount of time on mechanical ventilation without compromising patient comfort or level of sedation. Patients are randomized into a control arm (continuous infusion) and a trial arm (sliding scale hourly bolus) using versed for sedation and fentanyl for pain medication. Inclusion criteria are surgical patients requiring mechanical ventilation, including trauma patients, post operative patients, etc. Primary end point is total time of mechanical ventilation in each arm. Secondary end points are amount of medication given, time in ICU, time to discharge. Mortality and adverse events in both arms are recorded and reported to the Institutional Review Board for monitoring.

NCT ID: NCT03176680 Not yet recruiting - Anesthesia Clinical Trials

The Effects on Major Organ Complications on Esophagectomy of New Anesthetic ERAS Strategy: a Prospective Investigation

ERAS
Start date: June 15, 2017
Phase: N/A
Study type: Interventional

The goals of this study are to testify the effectiveness on enhancement recovery by new anesthetic ERAS (Enhanced recovery after surgery) strategy.

NCT ID: NCT03174223 Completed - Pneumonia Clinical Trials

Influence of Deep Versus Moderate Neuromuscular Blockade During General Anesthesia on 30-day Readmission Rates

Start date: June 1, 2017
Phase:
Study type: Observational

Deep neuromuscular block (NMB) has shown to produce superior surgical conditions during various abdominal and non abdominal surgeries. It is however unknown if the application of deep NMB leads to favourable outcome, such as lower rate of postoperative complications in general and surgical infections in specific and ultimately lower readmission rates. In the leiden university medical center, deep NMB is routinely applied for a variety of procedures, most notably laparoscopic abdominal and retroperitoneal surgery, eye surgery and neuro radiologic intervention surgery, since 2014. This retrospective study intends to investigate whether the application of deep NMB for these procedures affects patient outcome and readmission rates.

NCT ID: NCT03172182 Completed - Anxiety Clinical Trials

Perioperative Effects of Operating Room Virtual Tour

Start date: August 1, 2017
Phase: N/A
Study type: Interventional

Preoperative anxiety is associated with adverse consequences such as emergence delirium, and postoperative behavioral changes. According to previous studies, providing information of anesthetic procedures helps to lessen preoperative anxiety. However, verbal explanation alone provides the limited effect, and the tour program of the operating room prior to surgery may not be possible for a number of hospitals due to organizational and financial reasons. Therefore, the virtual reality (VR) tour of the operating room may be an innovative and novel method to give children information about the preoperative process and to alleviate the preoperative anxiety. In this study, we intend to evaluate the effects of the operating room virtual tour on preoperative anxiety as well as emergence delirium and postoperative behavioral changes, in pediatric patients.

NCT ID: NCT03171766 Recruiting - Clinical trials for Postoperative Complications

Pre-operative Neurocognitive Disorder and Low Near-infrared Spectrometry is Associated With Postoperative Delirium

Start date: June 15, 2017
Phase: N/A
Study type: Observational

The main goal of the investigation is to identify the incidence of cognitive dysfunction and POD in patients older than 65 years of age undergoing neurosurgical elective surgery and determine if an association between cognitive dysfunction, basal NIRS and POD exists.

NCT ID: NCT03169998 Completed - Liver Diseases Clinical Trials

Effect of Goal-directed Fluid Therapy on Postoperative Complications

Start date: January 1, 2017
Phase:
Study type: Observational

- It has been known that the recent application of a goal-directed fluid therapy (GDFT) to the intraoperative fluid infusion in patients contributes to decreasing the prevalence of postoperative complications and shortening the length of study in the intensive care unit as well as hospital stay compared with conventional methods. - Laparoscopic surgery is in a trend that its application is being expanded recently, but there has been no report on the application of GDFT to laparoscopic surgery so far. - To this end, this study aims to apply the intraoperative GDFT protocol in patients undergoing laparoscopic hepatobiliary or pancreatic surgery and to find out whether there is any difference in postoperative recovery and incidences of postoperative complications, by comparing with patients applied with the fluid therapy using existing conventional methods

NCT ID: NCT03165760 Completed - Clinical trials for Postoperative Complications

Protective Mechanical Ventilation and Risk of Postoperative Complications in Abdominal Surgery

Start date: July 1, 2015
Phase: N/A
Study type: Interventional

Randomized controlled trial, comparing two groups of 40 patients each scheduled for open major abdominal surgery. The intervention group was ventilated with a protective strategy consisting on a low Tidal volume (Vt) (6ml/kg of predicted body weight (PBW)), positive end expiratory pressure (PEEP) = 10 cm H2O and recruitment manoeuvres (RM) after disconnection from the ventilator, the control group had classic ventilation (Vt = 8 ml/kg of PBW, PEEP = 4 cmH2O and no RM).

NCT ID: NCT03164408 Completed - Clinical trials for Implant Complication

Orthopaedic Implant Removal

Start date: January 1, 2014
Phase: N/A
Study type: Observational

The necessity of orthopedic implant removal is under intense discussion and even if it is performed as an elective procedure, the risk of complications is present. Aim of the study is to identify parameters responsible for an increased risk of early post-operative complications after elective aseptic orthopedic implant removal.

NCT ID: NCT03163563 Completed - Clinical trials for Perioperative/Postoperative Complications

Perioperative Hypothermia Hypothermia in Ambulatory Surgery

Start date: March 2016
Phase: N/A
Study type: Observational

The purpose of the study is to measure patient- temperature in the perioperative period of patients undergoing plastic surgery in an ambulatory surgical unit. This study will evaluate if active warming with self-warming blanket (Easywarm®) is as effective as active warming with forced-air blanket (BairHugger®). Second the study will evaluate if one or both methods is effective in preventing perioperative hypothermia.