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Critical Illness clinical trials

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NCT ID: NCT03793244 Completed - Critical Illness Clinical Trials

TARGET-Metabolic Effects

TARGET-ME
Start date: July 1, 2017
Phase:
Study type: Observational

The estimation of calorie needs during routine practice in critically ill patients is highly variable and the thermogenic effect of continuous delivery of enteral nutrition (EN) on overall calorie utilisation in critically ill adults is unknown. The TARGET-ME study is a substudy of the TARGET trial (NCT02306746). The TARGET trial provides the perfect opportunity to measure calorie utilisation via indirect calorimetry (IC) and ventilator-derived carbon dioxide production (VCO2) to compare measured calorie utilisation to estimation methods, determine the potential thermic effect of EN solutions with different energy concentrations and investigate any associations with outcome.

NCT ID: NCT03789396 Completed - Critical Illness Clinical Trials

Pilot Study of Targeted Normoxia in Critically Ill Trauma Patients

Start date: January 1, 2018
Phase:
Study type: Observational [Patient Registry]

The objective of this study is to conduct an observational pre/post study to evaluate the clinical impact oxygen guideline implementation on oxygen utilization and oxygenation in critically ill trauma patients.

NCT ID: NCT03789305 Completed - Critical Illness Clinical Trials

Differences in Frail and Non-frail Critically-ill Patients in Functional Outcomes

DEFAULT
Start date: April 1, 2017
Phase:
Study type: Observational

This is a prospective analysis of patient registry data of intensive care patients. The aim is to investigate if frailty is a predictor of decline of functional status of critically ill patients during their hospital stay.

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: NCT03785444 Completed - Critical Illness Clinical Trials

Comparison of Self-assessment vs. Assessment by Others of Critically Ill Patients

ASTON
Start date: February 25, 2019
Phase:
Study type: Observational

We will test the results of standardized questionnaires for patients admitted to intensive care assessed by relatives/caregivers compared to the patient itself. Furthermore we will compare results with patients not admitted to intensive care.

NCT ID: NCT03781713 Completed - Critical Illness Clinical Trials

Prospective Clinical Surveillance With Application of Trigger Tools in Critically Ill Patients

Start date: November 1, 2017
Phase: Phase 2
Study type: Interventional

This study evaluates the impact of prospective clinical surveillance with the use of triggers to identify risk of adverse events with prompt adoption of interventions on the stabilization time of critically ill patients.

NCT ID: NCT03776409 Completed - Critical Illness Clinical Trials

Safety and Efficacy of Vancomycin Plus Beta-lactams

SEVPB
Start date: December 12, 2018
Phase:
Study type: Observational

The combination of vancomycin and piperacillin-tazobactam has been associated with an increased risk of acute kidney injury (AKI) in non-critically ill patient populations, but it is still unknown if this association exists in critically ill patients. The objective of this study is to compare AKI and efficacy of vancomycin plus piperacillin-tazobactam or beta-lactams.

NCT ID: NCT03771014 Completed - Critical Illness Clinical Trials

A Feasibility Study of Early Mobilisation Programmes in Critical Care

EMPRESS
Start date: May 28, 2019
Phase: N/A
Study type: Interventional

The objective of this study is to determine the feasibility of delivering a very early mobility rehabilitation program in Intensive Care Units (ICU), within the context of a randomised controlled trial (RCT). This will inform the design of a future RCT investigating very early ICU rehabilitation in the UK National Health Service.

NCT ID: NCT03767127 Completed - Anemia Clinical Trials

Oxygen Extraction-guided Transfusion in Critically Ill Patients

Start date: July 1, 2017
Phase:
Study type: Observational

Anemia is common in intensive care unit (ICU) patients and often appears early in the ICU course. The optimal management red blood cells RBC transfusion in critically ill patients remains controversial and clinical studies in this field have usually been based on transfusion thresholds. In the "TRICC" Trial, patients assigned to a restrictive transfusion strategy (transfusion if Hb<7 g/dL) had similar mortality to patients transfused if Hb<10 g/dL. Notably, none of the large RCT tried to focus on a personalize RBC transfusion protocol, i.e. a transfusion protocol which address the individual need for transfusion basing on physiological approach. We therefore hypothesized that patients with high extraction of oxygen could benefit more of RBCs transfusion regardless their hemoglobin levels.

NCT ID: NCT03749330 Completed - Critical Illness Clinical Trials

Improving Family Meetings in the Pediatric Cardiac Intensive Care Unit

Start date: December 19, 2018
Phase: N/A
Study type: Interventional

This study aims to improve communication between medical teams, patients, and families in the pediatric cardiac intensive care unit. The researchers hypothesize that both improving interprofessional teamwork when preparing for family meeting and preparing families for these meetings will improve team and family satisfaction with communication. The study will involve bringing together a group of medical professionals and parents of patients to collaboratively design an intervention. In addition, the researchers will study feasibility and acceptability of the intervention and whether it impacts family and team outcomes.