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Critical Illness clinical trials

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NCT ID: NCT03732443 Withdrawn - Critical Illness Clinical Trials

FAM-CAM Translation and Validation Into German

TRAVAGE-FAM
Start date: January 1, 2019
Phase:
Study type: Observational

Validation and Translation of the Family Confusion Assessment Method (FAM-CAM) into German according to Principles of Good Practice for the Translation and Cultural Adaptation Process for Patient-Reported Outcomes of the International Society for Pharmaoeconomics and Outcome Research and comparison to CAM-ICU.

NCT ID: NCT03730844 Completed - Critical Illness Clinical Trials

Functional Outcomes in Children Post Critical Illness

Start date: April 13, 2015
Phase:
Study type: Observational

Improvements in medical care have led to decreasing mortality rates in critically ill children, which have been reported to be as low as 5%. However, surviving critical illness does not necessarily translate to a return to pre-critical illness functional and developmental levels. Adult literature has shown that critical illness increases functional disability for up to five years post intensive care unit stay. We hypothesize that children experience similar functional disabilities as a result of critical illness, which may, as in adults, be primarily due to muscle wasting. The aim of this prospective observational pilot study is establish the relationship between intensive care unit stay and functional outcomes in pediatric survivors of critical illness.

NCT ID: NCT03727165 Withdrawn - Critical Illness Clinical Trials

Nocturnal Cyclic Enteral Nutrition Infusion Versus Continuous Infusion of Enteral Nutrition

Start date: December 11, 2018
Phase: N/A
Study type: Interventional

Enteral nutrition is considered the best way to feed those who can´t be fed orally. the standard protocol of administration includes continuous infusion for 24 hours; nonetheless this support is constantly suspended which causes a decrease in the nutrition administered vs the one formulated. Therefore this randomized clinical trial attempts to compare de standard administration vs. cyclic infusion during night hours measuring the formulated vs the administered volume of enteral nutrition given to the patient. The control group will be assigned standard 24 hour infusion of enteral nutrition while the experimental group will be assigned cyclic infusion during night hours. The variables include volume formulated, volume given in 24 hours, hours and reasons why the enteral nutrition was suspended, and related complications (abdominal distension, vomiting, and diarrhea).

NCT ID: NCT03726086 Completed - Critical Illness Clinical Trials

Post-extubation Assessment of Laryngeal Symptoms and Severity

PALSS
Start date: February 12, 2019
Phase:
Study type: Observational

The goal of this study is to learn more about voice and airway problems that patients experience during and after the time patients have an oral endotracheal tube in patients' airway to help patients breathe while receiving mechanical ventilation in an intensive care unit (ICU).

NCT ID: NCT03717831 Completed - Critical Illness Clinical Trials

Muscle Dysfunction in Critical Illness

Start date: October 17, 2018
Phase:
Study type: Observational

Patients surviving critical illness suffered significant skeletal muscle dysfunction and weakness that impacts their functionality and independence. The primary purpose of this project is to develop a classification system based on the health and function of the muscle at very early time points during critical illness. The investigators will determine if muscle ultrasound can predict functional recovery at six-months post hospital discharge. Researchers will assess muscle health and function from starting day one of admission to ICU and continue until six months of recovery. In addition to muscle ultrasound, the investigators will assess muscle strength and power, and perform muscle tissue analysis on a subset of individuals. These findings will be correlated to physical function and independence at six-month follow-up.

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: NCT03714399 Completed - Surgery Clinical Trials

Muscle Recovery Following Aortic Surgery Induced ICUAW.

VARIANCE
Start date: February 19, 2019
Phase:
Study type: Observational

To identify determinants of 'good and bad recovery' from ICUAW and build knowledge around the timing of these processes. Also, the investigators want to discover the effects of ICUAW on physical function and HRQoL following aortic surgery.

NCT ID: NCT03709589 Completed - Critical Illness Clinical Trials

Comparison of Mortality Among HDU Patients With Modified Early Warning Score Cutoff of 5

Start date: December 6, 2018
Phase:
Study type: Observational

Early categorization of critically ill patients by calculating MEWS score in hospitals may give a time window for appropriate steps. If a patient is suffering from sepsis, timely intravenous fluids, early antibiotics and monitoring in a low resource country like Pakistan, may have a great impact. Therefore, the current research is planned to early identify critically ill patients by applying MEWS and reducing the mortality by providing early management and taking appropriate life saving measures. Objective: To compare frequency of mortality on 7th day of admission in HDU patients with Modified Early Warning Score at the time of admission of < 5 & ≥ 5.

NCT ID: NCT03698292 Recruiting - Clinical trials for Critically-ill Patients

Itopride in Feeding Intolerance of Critically-ill Patients Receiving Enteral Nutrition

Start date: October 2018
Phase: N/A
Study type: Interventional

The current study will compare the effectiveness as well as the safety of Itopride against metoclopramide as the first line treatment for feeding intolerance in critically ill patients.

NCT ID: NCT03683511 Completed - Pharmacokinetics Clinical Trials

Nomograms for Optimization of Amikacin First Dose in Critically Ill Patients Using a Population Pharmacokinetics Model

PIC-AMI
Start date: April 21, 2014
Phase:
Study type: Observational

The aim of this study is to elaborate nomograms to optimize amikacine first dosing in critically ill patients, using a population pharmacokinetics model elaborated with multicentric data.