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Perioperative Care clinical trials

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NCT ID: NCT03328039 Completed - Perioperative Care Clinical Trials

uSing Wearable TEchnology to Predict Perioperative High-riSk Patient Outcomes

STEPS
Start date: February 1, 2017
Phase:
Study type: Observational

This is an observational, non-interventional study to assess the equivalence of wearable monitors with formal CPET testing for the prediction of physiological reserve before major surgery.

NCT ID: NCT03325413 Completed - Perioperative Care Clinical Trials

Improvement of Perioperative Care of Elderly Patients

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

The focus of this study is the development of a perioperative treatment concept for elderly patients, based on individual necessities and risk factors, aiming to improve patient outcome. The planned interventions include preoperative screening for malnutrition, frailty and uncalled-for long-term medication, if required followed by early prophylaxis and treatment of these risk factors, prior to or during surgery.

NCT ID: NCT03308071 Completed - Postoperative Pain Clinical Trials

Hypnosis for Symptom Management in Elective Orthopedic Surgery

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

The purpose of the study is to determine if teaching self-hypnosis techniques to patients prior to knee replacement surgery will decrease their pain medication requirements, pain medication side-effects, length of stay in the hospital, readmission rates, pain, anxiety, physical function, satisfaction scores, and cost of admission.

NCT ID: NCT03189550 Completed - Colorectal Surgery Clinical Trials

Enhanced Recovery After Surgery in Colorectal Surgery: A Large-Scale Quality Improvement Project

ERAS
Start date: July 1, 2014
Phase:
Study type: Observational

Multimodal perioperative care pathways have evolved into enhanced recovery after surgery (ERAS). ERAS pathways improve the quality of patient care, reduce morbidity, and shorten length of stay. This project will test the hypothesis that implementation of a multi-modal ERAS perioperative care protocol in colorectal surgical patients will result in significantly reduced perioperative morbidity and mortality.

NCT ID: NCT03111875 Completed - Clinical trials for Surgery--Complications

Perioperative Hypothermia and Myocardial Injury After Non-cardiac Surgery

PROTECT
Start date: March 27, 2017
Phase: N/A
Study type: Interventional

We propose to test the hypothesis that aggressive warming reduces the incidence of major cardiovascular complications, compared to routine care. Half of the participants will be randomly assigned to routine care (core temperature ≈35.5°C), while the other half will receive aggressive warming (>37°C core temperature) in a multi-center trial.

NCT ID: NCT03012802 Completed - Clinical trials for Postoperative Complications

Postoperative Outcomes Within an Enhanced Recovery After Surgery Protocol

POWER
Start date: September 15, 2017
Phase:
Study type: Observational [Patient Registry]

Short title POWER Audit Methods 60 days national (Spain) audit of postoperative complications following elective gastrointestinal surgery within an enhanced recovery after surgery (ERAS) protocol. Research sites Hospitals undertaking elective lower gastrointestinal surgery. Objective To provide detailed data describing post-operative complications and associated mortality; and length of stay. To provide detailed data describing adherence to ERAS protocol and its association to morbidity. Number of patients Not specified. All eligible patients undergoing surgery during the study month. Inclusion Criteria All adult patients (aged ≥18 years) undergoing lower gastrointestinal elective surgery within an ERAS protocol during the 60 day study period. Statistical analysis Univariate analysis will be used to test factors (patient, surgical, and ERAS related) associated with surgical complications, length of stay (LOS) and in-hospital death. Single and multi-level logistic regression models will be constructed to identify factors independently associated with these outcomes and to adjust for differences in confounding factors. A stepwise approach will be used to enter new terms. A single final analysis is planned at the end of the study. Summary statistics with post hoc Bonferroni corrections will be used to assess possible dose-response dependence in percentage of patients with postoperative complications and LOS. Proposed Start Date A 60 day period between 2017 Proposed End Date Data collection will end by September 2017 Study Duration Six months

NCT ID: NCT02768610 Completed - Perioperative Care Clinical Trials

Use of Preanesthetic Dexmedetomidine in Elderly, Treated-hypertensive Patients

Start date: March 2016
Phase: Phase 4
Study type: Interventional

Background: Dexmedetomidine is an alpha 2 adrenergic agonist with sedative, anxiolytic, and analgesic properties. This study was designed to evaluate the inhibitory effects of preoperative 0.5 μg/kg dexmedetomidine on hemodynamic responses caused by endotracheal intubation in elderly patients being treated for hypertension. Methods: Forty elderly (≥ 65 years) treated-hypertensive patients of American Society of Anesthesiologists physical status II undergoing elective noncardiac surgery were randomly and assigned to two groups. Group C received normal saline and group D received 0.5 μg/kg dexmedetomidine intravenously over 10 min just before endotracheal intubation. Systolic blood pressure (SBP), diastolic blood pressure (DBP), mean arterial pressure (MAP) and heart rate (HR) were recorded preoperatively at ward, immediately after study drug administration, and at 1, 3, and 5 minutes after endotracheal intubation.

NCT ID: NCT02580214 Completed - Perioperative Care Clinical Trials

Immunonutrition in Total Hip Arthroplasty

Immunehip
Start date: May 2013
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this pilot study was to investigate whether the use of a multimodal protocol of preoperative care plus preoperative immune nutrition would decrease the length of stay and acute phase inflammation in patients submitted to total hip arthroplasty (THA). The study was designed to be randomized and controlled, but not double blind. The patients were randomized to receive either preoperative care based on evidence plus immune nutrition for 5 days prior to surgery (Acerto group) or traditional preoperative care (control group). Main endpoints were length of stay and acute-phase postoperative response

NCT ID: NCT02527967 Completed - Colonic Neoplasms Clinical Trials

ERAS in Laparoscopic Surgery for Colorectal Cancer: Risk Factors for Delayed Recovery

Start date: January 2013
Phase: N/A
Study type: Observational

Although there is evidence for reducing complication rate and improving recovery after the implementation of Enhanced Recovery After Surgery (ERAS) protocols into colorectal surgery, most published papers include patients undergoing open resections. The aim was to analyse factors affecting recovery and length of stay (LOS) in patients after laparoscopic colorectal surgery for cancer combined with ERAS protocol.

NCT ID: NCT01607177 Completed - Obesity Clinical Trials

Do Text Message Reminders Increase Preoperative Exercise in Obesity Surgery Candidates?

Start date: August 2012
Phase: Phase 3
Study type: Interventional

Preoperative exercise has been shown to improve physiological and functional capacity in patients undergoing abdominal surgery to prepare them for the stress of surgery. Patients undergoing bariatric surgery are advised to partake in regular preoperative exercise. In the setting of bariatric surgery, as well as preparing patients for the stress of surgery, it is also thought to increase the likelihood that they will exercise postoperatively. However, compliance to this advice is extremely low. Text-message interventions have been shown to improve compliance to other lifestyle interventions. The investigators will compare the rate of compliance to preoperative exercise prior to bariatric surgery in patients who receive a daily text message to those who do not. The investigators will also compare weight loss.