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Postoperative Complications clinical trials

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NCT ID: NCT03114306 Completed - Postoperative Pain Clinical Trials

Evaluation of a Fast-track Knee Arthroplasty Concept

KneeOptOut
Start date: April 5, 2017
Phase: N/A
Study type: Interventional

Mobilisation following knee arthroplasty is an important aspect to achieve early and enhanced recovery after surgery and sufficient joint function. Analgesia is a crucial therapeutic element in this context. This RCT evaluates two analgetic regimens for patients undergoing primary total knee-replacement to assess impact on postoperative recovery.

NCT ID: NCT03110185 Completed - Clinical trials for Postoperative Complications

Postoperative Delirium: Brain Vulnerability and Recovery

Start date: November 25, 2015
Phase: N/A
Study type: Interventional

In this study, we propose to use EEG and a brain imaging technique known as diffuse optical tomography (DOT) to study when people are in delirium and when they recovery. We plan to also compare brain function of patients who recovered from delirium to patients who did not have delirium using DOT and fMRI. We will also continually monitor the participant's EMR to help coordinate timing of study procedures, as well as to collect information pertaining to their surgery, recovery progress, and indicators of mental status including delirium.

NCT ID: NCT03109418 Terminated - Clinical trials for Obstructive Sleep Apnea

Intraoperative Low-dose Ketamine Infusion for Patients With Obstructive Sleep Apnea

Start date: June 2, 2016
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this study is to substantially reduce overall postoperative morbidity and mortality associated with obstructive sleep apnea.

NCT ID: NCT03107572 Completed - Clinical trials for Postoperative Complications

Predictive and Prognostic Value of Cellular Dysoxia Markers After Cardiac Surgery With Extracorporeal Circulation

Start date: June 2016
Phase:
Study type: Observational

The study consist of evaluation in cardiac surgery with cardiopulmonary bypass (CPB) setting the ability of PCO2 derived variables (ΔPCO2, ΔPCO2/C(a-v)O2 ratio), compared to lactate and ScVO2 to predict major postoperative adverse events.

NCT ID: NCT03102619 Completed - Clinical trials for Postoperative Complications

Wireless Assessment of Respiratory and Circulatory Distress; A Pilot Study

WARD
Start date: March 23, 2017
Phase: N/A
Study type: Observational

Postoperative observation of patients is based on the Early Warning Score (EWS). By using continuous wireless monitoring of vital parameters it may be possible to predict the risk of complications after abdominal cancer surgery. The object of this pilot study is to test the equipment and methods for the next phases. Patients will be monitored for 4 days postoperatively and data is analyzed retrospectively. Vital parameters are monitored with ECG, blood pressure monitor and pulseoximetry. In the analysis the investigators will compare the results from the continuous monitoring to the measurements made by the nurses and registered in the EWS. The primary outcomes for the pilot study are the frequency of measurements resulting in a single parameter score of 3 according to the EWS algorithm.

NCT ID: NCT03094988 Completed - Clinical trials for Cognitive Impairment

COgnitive and Physical Exercise (COPE) Prehabilitation Pilot Feasibility Study

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

Cognitive and functional impairment are debilitating problems for survivors of major surgery. Efforts to modify medical treatments to prevent such impairment are ongoing and may yet yield significant benefits. An area in need of study is whether building patients' cognitive and physical reserve through a prescribed program of cognitive and physical exercise before the physiological insult (a prehabilitation effort) can improve long-term outcomes. Prehabilitation efforts before surgery thus far have focused on preemptive physical therapy to improve post-surgical functional outcomes. No work, however, has been done to attenuate the cognitive decline commonly seen after surgical illness by exercising the brain before the surgical insult. Cognitive prehabilitation is a novel therapeutic approach that applies well-understood techniques derived from brain plasticity research. Our approach is bolstered by data that demonstrate that cognitive training programs are effective and have a very high likelihood of fostering improvement in patient outcomes across a range of populations. It is not yet known if these programs can improve cognitive reserve, allowing patients' minds to better manage the acute stress of surgery and hospitalization. The primary aim of this pilot study is to evaluate the feasibility of cognitive and physical prehabilitation training in adult patients undergoing major non-cardiac surgery who are at risk for postoperative cognitive and functional decline. The secondary aim is to study the effects of cognitive and physical prehabilitation training on cognitive abilities, functional status, and quality of life after surgery.

NCT ID: NCT03092401 Active, not recruiting - Liver Cirrhosis Clinical Trials

Hepatopulmonary Syndrome and Postoperative Complications After Liver Transplantation : A Case-control Study

HPS
Start date: October 1, 2015
Phase: N/A
Study type: Observational

Hepatopulmonary Syndrome is a respiratory complication of liver cirrhosis defined as a triad: hypoxemia (PaO2 < 80 mmHg in room air), chronic liver disease and intrapulmonary vasodilatations. Its prevalence varies between 4 and 32%. Numerous treatments have been tried but the only efficient therapy to cure the syndrome is liver transplantation. Without transplantation it is associated with a higher mortality which is the reason why hepatopulmonary syndrome patients have a higher priority to transplantation. However it appears in some restricted studies that hepatopulmonary syndrome is associated with more postoperative complications (infections, vascular and biliary complications, prolonged length of mechanical ventilation…). The investigators hypothesised that hepatopulmonary syndrome patients have more postoperative complications after liver transplantation than non hepatopulmonary syndrome patients matched on age, MELD (Model for End-Stage Liver Disease) score, comorbidities, perioperative transfusion and noradrenaline doses.

NCT ID: NCT03084809 Completed - Colorectal Cancer Clinical Trials

Chemotherapy Combined With CIK Treating Colon Cancer

Start date: May 6, 2012
Phase: Phase 4
Study type: Interventional

Cytokine-induced killer cells (CIK) is an auxiliary antitumor treatment. The investigators aim to evaluate the clinical efficacy of chemotherapy combined with CIK in the treatment of postoperative colorectal cancer patients. And to provide useful reference for the clinical application of CIK in colorectal cancer patients.

NCT ID: NCT03067259 Completed - Clinical trials for Postoperative Complications

Post Operative Cognitive Dysfunction

POCD
Start date: February 20, 2017
Phase: N/A
Study type: Interventional

The objective of this study will be to estimate the incidence of postoperative cognitive dysfunction (DCPO) in patients over 65 years of age, undergoing surgical / anesthetic procedures and in patients who will not undergo surgical / anesthetic. The patients will be taken from the Hospital Italiano de Buenos Aires.

NCT ID: NCT03060837 Recruiting - Clinical trials for Perioperative/Postoperative Complications

Investigate the Renal Movement by Single Lung Ventilation in Patients Administered RIRS for Kidney Stones.

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

In patients undergoing RIRS for kidney stone, we aim to show the effect of single lung ventilation with a double lumen tube on operative (operation scope duration, perforation, hemorrhage, etc. complications) and postoperative parameters (stone-free rates, complications like postoperative hemorrhage and fever, hospital stay, etc.) and to show changes in renal stone position during simultaneous normal ventilation and single lung ventilation.