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Critical Illness clinical trials

View clinical trials related to Critical Illness.

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NCT ID: NCT02865408 Recruiting - Inflammation Clinical Trials

Amino Acid Nutrition in the Critically-ill

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

Enhancing the anabolic effect of nutrition in critically ill patients by administering exogenous amino acids.

NCT ID: NCT02837419 Recruiting - Critically Ill Clinical Trials

Cost-effectiveness of Extracorporeal Life Support Treatment

Start date: December 1, 2017
Phase:
Study type: Observational [Patient Registry]

This study evaluates patients on ECLS treatment as considered appropriate with mortality and health related Quality of life and costs.

NCT ID: NCT02804438 Recruiting - Critical Illness Clinical Trials

Establishing Normative Data for Pupillometer Assessments in Neuro-Intensive Care

ENDPANIC
Start date: July 2015
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to collect a large amount of data that may assist in addressing the gap in knowledge of understanding pupillometer readings using a pupillometer device. The aim of this project is to establish normative values for pupillometer data. Measures of central tendency will be developed for the variables provided by automated pupillary exams, which will provide an enhanced understanding of clinically appropriate pupil values for size, reactivity, and neurological pupil index.

NCT ID: NCT02790697 Recruiting - Critical Illness Clinical Trials

The ICALIC Accuracy Validation in Geneva Study

ICALIC
Start date: September 10, 2017
Phase:
Study type: Observational

This study aims at validating the accuracy of the new indirect calorimeter (Q-NRG, COSMED, Italy), developed for the ICALIC multicenter study. The validation of accuracy will only be conducted in Geneva center. The measurements made with the new calorimeter will be compared to the measurements by the mixing chamber method using a mass spectrometer (MAX300-LG, Extrel, USA) for gas composition analysis.

NCT ID: NCT02766166 Recruiting - Critical Illness Clinical Trials

Critical Health Assessment and Outcomes Score/Study

CHAOS
Start date: September 1, 2019
Phase:
Study type: Observational

CHAOS is based on the investigator's new and exciting results from pre-clinical and large longitudinal multi-center observational clinical studies of critically ill patients and asymptomatic community-based adults with little or no advanced disease. By integrating approaches from the physical, biological, computational, statistical and clinical sciences, this observational study will test the hypothesis that early diagnosis of subclinical signatures of critical illness encoded within physiological signals complements conventional clinical predictors by providing unique prognostic insight. The primary goal is to reduce mortality, morbidity and complications by early identification of individuals with brewing subclinical critical illness and adverse events before overt clinical presentation (e.g., cardiac arrest, arrhythmias, hemorrhage, respiratory failure, circulatory collapse). This will provide the necessary lead time for healthcare providers to deliver early, more effective and/or preventive therapies. Through innovative approaches, CHAOS also meets the challenge of medical errors to reduce missed diagnosis, misdiagnosis, preventable harm and variability in provider adherence to best practice guidelines. The goal is to validate predictive algorithms and identify subclinical signatures of illness, ranging from asymptomatic adults in the community to very sick patients in the hospital. The overall goal is to make healthcare more precise, effective, efficient, safe and timely while reducing costs, preventable harms and adverse events.

NCT ID: NCT02763709 Recruiting - Clinical trials for Critical Illness Polyneuropathy

Evaluation of Pediatric Critical Illness Neuropathy/Myopathy in Pediatric Intensive Care Unit

Start date: March 2016
Phase: N/A
Study type: Observational

Intensive Care Unit Acquired Weakness(ICUAW) encompasses a spectrum of disorders characterized by generalized weakness developing after the onset of critical illness. Pediatric data on the incidence of ICUAW is restricted to isolated case reports and case series of no more than five children. Critical illness polyneuropathy is characterized by reduction in compound motor action potential or sensory nerve action potential or both with preserved conduction velocity on electrophysiological studies. These findings can occur very early prior to the onset of clinical features. Given the dearth of data in children on the subject, this study has been planned to evaluate the incidence of critical illness associated polyneuropathy /myopathy in severely sick children admitted.

NCT ID: NCT02731898 Recruiting - Clinical trials for Acute Respiratory Failure, Mechanical Ventilation, Critically Ill Patients, Mortality

Fourth International Study of Mechanical Ventilation From VENTILA GROUP

ISMV
Start date: April 28, 2020
Phase:
Study type: Observational

A prospective, international and multicenter, non interventional single-cohort study, which will enroll consecutive adult patients who have received mechanical ventilation (invasive and noninvasive ventilation) for at least 12 hours during a 1-month period, and will follow each patient for the duration of mechanical ventilation, up to 28 days. The main objectives will be to analyze the mortality and clinical outcomes in ventilated patients and secondly, to evaluate the practices of liberation from mechanical ventilation, the failure of non invasive ventilation in the ICU, and to analyze the clinical outcomes in specific populations of critically ill patients with the need of mechanical ventilation.

NCT ID: NCT02730221 Recruiting - Critical Illness Clinical Trials

Administrative Workload in the Intensive Care Unit

AWIC
Start date: January 2016
Phase:
Study type: Observational

A prospective observational study in the Intensive Care Unit and the Medium Care Unit in a university hospital in Amsterdam. Recent studies show that administrative tasks occupy more than 30% of the workload. One-third of these administrative tasks is unrelated to care. The administrative workload of physicians and nurses will be observed and quantified using two different methods. The amount of time physicians and nurses are logged on into the patient data management system (PDMS) will be measured and the time spent on different work tasks will be monitored with a work sampling method. Two different patient data management systems will be compared.

NCT ID: NCT02706587 Recruiting - Clinical trials for Polyneuropathy, Critical Illness

Neuromuscular Electrical Stimulation for Intensive Care Unit-acquired Weakness Assessment

ENS
Start date: March 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether early neuromuscular electrical stimulation is effective in the prevention of neuromuscular weakness in critical ill patients.

NCT ID: NCT02690090 Recruiting - Hemorrhage Clinical Trials

Safety Study of Enoxaparin Prophylaxis in Critically Ill Adults With Severe Renal Insufficiency

Start date: February 2014
Phase: Phase 4
Study type: Observational

The investigators study is the first step (a pilot study) in determining whether the manufacturer's recommended dose of a blood thinner called enoxaparin, in adults who are patients in an intensive care unit and have severely reduced kidney function (less than or equal to approximately 30% of their normal function) is safe with respect to the adverse effect of bleeding. The investigators hypothesis is that studying these patients, going forward in time, without interfering with their care, to eventually determine if this blood thinner is safe at reduced doses, is feasible.