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Postoperative Complications clinical trials

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NCT ID: NCT02158923 Recruiting - Clinical trials for Moderated-high Risk of Postoperative Pulmonary Complication

Individualized Perioperative Open Lung Ventilatory Strategy

iPROVE
Start date: September 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether individualized ventilatory management combining the use of low tidal volumes, alveolar recruitment maneuvers, individually titrated positive end-expiratory pressure and postoperative individualized ventilatory support will decrease postoperative complications, unplanned ICU readmissions, ICU and hospital length of stay and mortality compared to a standardized Lung Protective Ventilation (LPV) for all patients at risk.

NCT ID: NCT02158299 Recruiting - Clinical trials for Postoperative Complications

Contrast The Role of Avitene And OK-432 in Reducing Seroma Formation After Axillary Lymphadenectomy for Breast Cancer

Start date: October 2013
Phase: Phase 4
Study type: Interventional

After Axillary lymphadenectomy for breast cancer there are not few patients showed seroma formation and it can not be ignored.Investigators aimed to study two new methods of application of Microfibrillar Collagen Hemostat Flour and OK-432 to reduce seroma formation and to verify the efficacy and safety of these two applications.Try to prove them as beneficial supplements for axillary lymphadenectomy of breast cancer.

NCT ID: NCT02155868 Completed - Clinical trials for Postoperative Complications

Role of Cerebral Oximetry in Reducing Postoperative Morbidity Following Cardiac Surgery

Start date: June 2014
Phase: N/A
Study type: Interventional

Cerebral oximetry employing near-infrared spectroscopy (NIRS) is a non-invasive modality used to estimate regional cerebral oxygen content saturation (rSO2). Near-infrared spectroscopy has increasingly been used in perioperative setting of heart surgery and many studies have outlined an increased incidence of postoperative morbidity in patients with significant perioperative reductions in rSO2. Although a relationship between rSO2 reductions and adverse outcomes has been reported, there is not compelling evidence that interventions to correct rSO2 during cardiac surgery lead to improved clinical outcomes. Hypothesis of the study is that interventions to normalize intraoperatively decreased cerebral rSO2 would reduce the overall incidence of postoperative complications in high-risk cardiac surgery patients.

NCT ID: NCT02150486 Completed - Myocardial Injury Clinical Trials

Myocardial Injury and Postoperative Complications

MICOLON
Start date: June 2012
Phase: N/A
Study type: Observational

To determine whether perioperative myocardial injury is associated with adverse outcome in patients scheduled for major abdominal surgery.

NCT ID: NCT02143128 Completed - Postoperative Pain Clinical Trials

Efficacy Side-effect Score (ESS): Development and Evaluation of a New Tool for Patients After Surgery

ESScore
Start date: March 2014
Phase: N/A
Study type: Interventional

We hypothesized that better control of postoperative pain treatment and its side effects by monitoring ESS might influence the degree of mobility and morbidity in surgical patients and consequently reduce LOS. Thus, our aim was to validate the influence of recording ESS and the application of a "call-out algorithm" on LOS in two university hospitals in which the routine policy of registration of pain had not been adopted yet.

NCT ID: NCT02127099 Not yet recruiting - Clinical trials for Obstructive Sleep Apnea

The Incidence of Undiagnosed OSA Compared in Multi-ethic Races of Malaysia & the Associated Postoperative Complications

Start date: May 2014
Phase: N/A
Study type: Observational

Obstructive sleep apnoea (OSA) is a condition in which a person's sleep is disrupted with momentary periods of apnoea and hypopnoea. This occurs when there is a blockage to airflow. When this happens, the patient will snore, gasp or choke in the attempt to attain more oxygen. This results in disrupted sleep and the patient may even awake from sleep. It has been found that a great proportion of Malaysians have habitual snoring and with the increase in obesity over the years, it is a concern that OSA may be prevalent in Malaysia. However, it has been seen that OSA is commonly undiagnosed in patient. This poses a worry because these people can come in for surgery. Diagnosis of OSA before surgery is important in order to prepare for the complication related to OSA.

NCT ID: NCT02102217 Completed - Clinical trials for Postoperative Complications

the PRECious Trial: PREdiction of Complications

PRECious
Start date: December 2015
Phase: N/A
Study type: Interventional

20% of patients who undergo major abdominal surgery will have a major complication, which requires invasive treatment and is associated with increased mortality, morbidity, hospital stay and intensive care stay. A quality control algorithm after Major Abdominal Surgery (MAS) aimed at early identification of patients at risk of developing major complications can decrease associated morbidity and mortality. Literature studies show promising results for C-reactive protein as an early marker for postoperative complications, however clinical significance has yet to be determined. Here the investigators propose a randomized clinical trial in order to determine the effect of postoperative monitoring with standardized CRP measurements on postoperative morbidity and mortality, if CRP levels exceed 140 mg/L additional CT-scan imaging will be conducted.

NCT ID: NCT02096640 Not yet recruiting - Inflammation Clinical Trials

Postoperative Inflammation and Recovery After Tracheostomy

Start date: March 2014
Phase: N/A
Study type: Interventional

The main purpose of this study is to examine if there are differences in postoperative inflammation following percutaneous dilatation tracheostomy versus surgical tracheostomy in intensive care unit patients.

NCT ID: NCT02084862 Completed - Clinical trials for Tracheostomy Complications

Ultrasound Guided Percutaneous Tracheostomy Compared to Bronchoscopy Guided Percutaneous Tracheostomy

TRACHUS
Start date: March 2014
Phase: N/A
Study type: Interventional

TRACHUS trial is a randomized non-inferiority trial designed to evaluate the safety and efficacy of ultrasound guided percutaneous tracheostomy compared to bronchoscopy guided percutaneous tracheostomy.

NCT ID: NCT02084615 Enrolling by invitation - Clinical trials for Postoperative Complications

Prospective Study Investigating Aspirin and Intraoperative Blood Loss and Complications Following Inguinal Hernia Repair

Start date: August 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether aspirin taken in the perioperative period will increase the blood loss associated with open inguinal hernia repairs. A secondary purpose of this study is to determine if the aspirin administered in the perioperative period increases the risk of complications associated with open inguinal hernia repairs.