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Critically Ill clinical trials

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NCT ID: NCT03879564 Active, not recruiting - Pain, Postoperative Clinical Trials

Ketamine-fentanyl VS Fentanyl for Analgosedation in SICU

Start date: April 5, 2019
Phase: Phase 4
Study type: Interventional

This is a randomized, double-blinded study to evaluate the analgosedative effect of ketamine in a surgical intensive care unit. The patients who will receive continuous fentanyl infusion for either pain control or sedation will be recruited in this trial. Fentanyl will be titrated with initial loading doses of 20 mcg until the numeral rating scale(NRS) less than 4 or critical care pain observation tool (CPOT) less than 3 or Richmond agitation sedation score (RASS) -2-0. Then the patients will be randomised in to receive saline infusion in control group (Group C) or ketamine infusion in ketamine group (Group K). Ketamine will be administered with an initial bolus of 0.3 mg/kg followed by a perfusion of1.5 mcg/kg/min during the first 48 h. The dose of fentanyl will be protocolized adjusted according to NRS or CPOT or RASS. We tested the research hypothesis that low-doseketamine infusion is associated with a reduced fentanyl dose without increased vulnerability to its psychotropic effects.

NCT ID: NCT03868241 Completed - Critically Ill Clinical Trials

Coated Devices to Decrease Infection in the Intensive Care Unit

CRITIC
Start date: April 6, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Pilot explanatory, randomized, open label, controlled trial. Critically ill patients which will demand placement of invasive devices for organ support (endotracheal tube, central venous catheter and urinary Foley catheter) will be randomized 1:1 to receive coated (Bactiguard®) or habitual (non-coated) devices.

NCT ID: NCT03811730 Recruiting - Critically Ill Clinical Trials

The Diagnosis and Treatment System of Transesophageal Echocardiography in ICU

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

Transesophageal ultrasound offers imaging through the esophagus on the surface of the heart, with good image quality and unique advantages. However, no studies to date have examined its effect in critically ill patients in China.Therefore, the investigators aimed to compare the efficacy and safety of TEE with TTE. the investigators will conducte a Multi-center, prospective observational control study enrolling critically ill adult patients in several ICU in China .

NCT ID: NCT03793257 Recruiting - Cardiac Arrest Clinical Trials

The EXCEL Registry of Patients Requiring ECMO

Start date: February 1, 2019
Phase:
Study type: Observational [Patient Registry]

ECMO is associated with significant costs, risks and requires specialist training and expertise. EXCEL is a novel, high-quality, detailed prospective registry of patients requiring ECMO in Australia and New Zealand. The registry provides information on patient selection, complications, costs and patient reported outcome measures. EXCEL uses the Theoretical Domains Framework to identify evidence-practice gaps and explore barriers and enablers to tailor implementation of evidence

NCT ID: NCT03787810 Completed - Clinical trials for Acute Coronary Syndrome

Left Ventricular Dysfunction in Critically Ill Patients

LEVEDYCIP
Start date: May 28, 2018
Phase:
Study type: Observational

Left ventricular dysfunction is common in the critically ill. The aim of this study is to assess the incidence and prognosis of left ventricular dysfunction in critically ill patients.

NCT ID: NCT03746496 Completed - Critically Ill Clinical Trials

POC Analysis of IO Blood Samples Within Critically Ill Patients

Start date: May 3, 2017
Phase:
Study type: Observational [Patient Registry]

This study aims to investigate whether point-of-care (POC) analysis of intraosseous (IO) blood samples from critically ill emergency patients are accurate enough for emergency decision making, in comparison with arterial point-of-care samples.

NCT ID: NCT03714724 Completed - Critically Ill Clinical Trials

PEEP Levels on Intraabdominal Pressure and Hemodynamics in Critically Ill Patients

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

In this study, it was aimed to compare the effects of three different PEEP levels (0-4, 5-8, 9-12 cmH2O) on intraabdominal pressure and hemodynamic parameters of patients in intensive care unit.

NCT ID: NCT03681626 Completed - Critically Ill Clinical Trials

Does Tracheal Suction During Extubation in Intensive Care Unit Decrease Functional Residual Capacity

Start date: October 27, 2015
Phase: N/A
Study type: Interventional

Little is known about the procedure of extubation of patients admitted in Intensive Care Units (ICU). In particular, effects of tracheal suction during extubation have never been evaluated. Tracheal suction induces alveolar derecruitment in sedated patients under mechanical ventilation and is a major source of pain. The aim of this study was to evaluate the impact of tracheal suction during the extubation procedure of critically ill patients on the end-expiratory lung volume.

NCT ID: NCT03596853 Not yet recruiting - Critically Ill Clinical Trials

Progressive Mobilization With Dose Control and Training Load in in Critically Ill Patients

Start date: June 1, 2019
Phase: N/A
Study type: Interventional

Immobilization and bed rest of patients in intensive care units (ICU) increases their risk for muscle dysfunction and prolonged mechanical ventilation, leading to physical deconditioning and loss of functionality. Active mobilization is a therapeutic strategy that typically involves exercises in which the patient uses his or her own strength and muscular control, is a feasible, safe, and low-cost intervention to improve muscle dysfunction and disability in patients at the ICU. Despite scientific advances, the current description and prescriptions of exercises at the ICU remain incomplete with respect to the control and the description of the variables of training load (volume and intensity), programming, and progression.

NCT ID: NCT03539653 Recruiting - Critically Ill Clinical Trials

The Effect of Gastric Antrum Ultrasonography on Early Stage of Enteral Nutrition in Critically Ill Patients.

Start date: May 1, 2018
Phase:
Study type: Observational

The purpose of this study is to investigate the effect of Gastric Antrum Ultrasonography on Early Stage of Enteral Nutrition in Critically Ill Patients.