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Critically Ill clinical trials

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NCT ID: NCT04470973 Recruiting - Sepsis Clinical Trials

Pharmacokinetics of Amikacin and Cefuroxime in Critically Ill Patients.

PHARAOH
Start date: July 15, 2020
Phase:
Study type: Observational

Infections in critically ill patients are a major healthcare problem and an important source of morbidity and mortality. Since critically ill patients often have altered pharmacokinetics (PK) compared to non-critically ill patients there is a substantial risk that present standard dosing regimens of antibiotics lead to suboptimal outcomes for patients on the ICU or the ED. To prevent the risk of inadequate dosing in ICU patients, it is important to fully understand the PK of antibiotics in this vulnerable group in order to optimize the dosing regimens. With this study, the investigators will describe the pharmacokinetics of cefuroxime and amikacin in ICU and ED patients. A heterogeneous population of ICU and ED patients will be included to be able to find which factors might influence the pharmacokinetics of these drugs and to what extent. By using population modeling the investigators will simulate different dosing regimens and MIC values and compare probability of target attainment between each of these dose and MIC combinations. This will allow the investigators to optimize dosing regimens of cefuroxime and amikacin in critically ill patients.

NCT ID: NCT04357847 Recruiting - Covid-19 Clinical Trials

Assessment of Endothelial and Haemostatic Changes During Severe SARS-CoV-2 Infection

Covid-Thelium
Start date: April 9, 2020
Phase:
Study type: Observational

The outbreak at covid-19 is caused by the SARS-CoV-2 virus. This virus can be responsible for severe respiratory failure but also for extra-respiratory organ dysfunctions associated with severe inflammatory stress. The endothelium is an important structure of the blood vessels and is implicated in the organ failure of many patients admitted in intensive care units. It could be affected by the virus and its alteration may explain the organ dysfunction of covid-19 ICU patients as well as the thrombotic processes frequently obstructed in this infection.

NCT ID: NCT04190173 Recruiting - Critically Ill Clinical Trials

Efficacy of PRUcalopride in Critically Ill Patients With Paralytic ILeus

EPRUCIL
Start date: July 1, 2017
Phase: Phase 3
Study type: Interventional

Paralytic ileus is a common intestinal dysfunction in critically ill patients. There are still no established the effective medications except correcting the primary causes and prokinetics trial which limited in efficacy and potential adverse events.

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: 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.

NCT ID: NCT03531515 Recruiting - Sepsis Clinical Trials

Predictors of Reactive Thrombocytosis in Critically Ill Septic Patients

Start date: April 11, 2018
Phase:
Study type: Observational [Patient Registry]

Reactive or secondary thrombocytosis is defined as abnormally high platelet count (≥4,50,000 platelets per micro-liter) in the absence of chronic myeloproliferative disease. In critically ill patients reactive thrombocytosis is not uncommon during recovery phase and an association has been seen with poor outcome and increased risk of subsequent VTE. However, not all patients with infection respond with thrombocytosis. No study has enumerated the risk factors or predictors of reactive thrombocytosis in critically ill septic patients.

NCT ID: NCT03231540 Recruiting - Critically Ill Clinical Trials

The PREServation of MUScle Function in Critically Ill Patients (PRESMUS)

PRESMUS
Start date: September 2016
Phase: N/A
Study type: Interventional

This study evaluates the effect of whey protein enriched enteral nutrition in addition to exercise training on the preservation of muscle function in critically ill patients. One half of patients receive whey protein enriched enteral nutrition with a protein intake of 1.5 g/kg/day and the other half of patients receive standard enteral nutrition with a protein intake of 1 g/kg/day.

NCT ID: NCT03157245 Recruiting - Critically Ill Clinical Trials

Incidence of Deep Vein Thrombosis on Central Venous Catheters in the Post Operative Period of Carcinologic Surgery

THROMBOCAT
Start date: June 2, 2017
Phase: N/A
Study type: Observational

The objective is to determine the incidence of thrombosis on central venous catheters in patients hospitalized in a surgical critical care unit, in the immediate postoperative period of urological or digestive carcinological surgery, and receiving parenteral nutrition.

NCT ID: NCT03044223 Recruiting - Sepsis Clinical Trials

Monocyte Profiles in Critically Ill Patients With Pseudomonas Aeruginosa Sepsis

MIPSA
Start date: August 2014
Phase:
Study type: Observational

The present study focuses on patients with Pseudomonas aeruginosa (PSA) sepsis. The aim of the present study is to find out whether the M1 (pro-inflammatory) or M2 (anti-inflammatory) phenotype predominates in blood monocytes in critically ill patients with PSA-sepsis, and whether the severity of sepsis and outcome is associated with distinct monocyte phenotype and function.