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Critical Illness clinical trials

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NCT ID: NCT01354899 Completed - Critical Illness Clinical Trials

A Open Study to Evaluate the Performance of Dressing on Subject With High Risk of Skin Breakdown

Start date: May 2011
Phase: N/A
Study type: Observational

The rational for the study is to add a thin self-adherent dressing on critically ill patients. Evaluate if the dressing might protect the skin for further breakdown.Participants will be followed for the duration of hospital stay, an expected average of 5 days.

NCT ID: NCT01347801 Completed - Hypoglycaemia Clinical Trials

Mechanisms of Insulin Resistance in Critical Illness: Role of Systemic Inflammation and GLP-1

Start date: March 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the role of inflammation and the insulin regulating hormone GLP-1 during critical illness.

NCT ID: NCT01344265 Completed - Critically Ill Clinical Trials

The Correlation Between B-type Natriuretic Peptide (BNP) and Global End Diastolic Volume

Start date: June 2010
Phase: N/A
Study type: Observational

The investigators hypothesized that the serum B-type Natriuretic Peptide (BNP) level may be correlated with global end diastolic volume (GEDV) as measured by transpulmonary thermodilution technique (PiCCO). The rationale is that some animal studies have proven that BNP is released from ventricular myocardium in response to physical expansion. Such physical expansion can be measured by GEDV. If the hypothesis can be confirmed with our study, the serum level BNP can be used to monitor volume status of critically ill patient, instead of the invasive monitoring system.

NCT ID: NCT01330264 Completed - Clinical trials for Intracranial Pressure

Study of Intracranial Pressure (ICP) Monitoring in Critically Ill

SIM City
Start date: July 2009
Phase: N/A
Study type: Observational

The SIM City study seeks to explore for the variance in practice that is associated with nursing and medical care of patients with brain pressure (ICP) monitors. The underlying hypothesis is that there is not a consistent pattern of care throughout the U.S., rather, there is a wide range of practice patterns that are used to monitor and treat ICP.

NCT ID: NCT01327079 Completed - Critically Ill Clinical Trials

The Use of Methadone in Newborn Infants

Methadone
Start date: December 2010
Phase: Phase 1/Phase 2
Study type: Interventional

This proposed investigation will test the following hypotheses: 1) Enzymatic activity of CYP2B6 characterized by the formation clearance of methadone to EDDP (CLf,EDDP), is directly related to both gestational and postnatal age; 2) variations in the CYP2B6 gene (SNPs) are associated with variable activity of the CYP2B6 enzyme (as measured by the formation clearance, CLf,EDDP), and 3) the elimination rate of methadone and its major metabolite EDDP in neonates is dependent on the glomerular filtration rate and therefore on the stage of development (defined by both gestational and postnatal age). The investigators propose to develop a PK model for methadone dosing in neonates that takes into account both developmental stage and genetic variability. The long-term goal of the proposed investigations is to improve dosing of methadone in neonates exposed to opioids in utero or post-natally, leading to improved control of their withdrawal syndrome and decreased adverse drug reactions associated with the current use of methadone in these vulnerable patients. More immediately, the investigators will develop a PK model for methadone dosing based on relevant developmental and genetic characteristics. The acquired knowledge based on the proposed study will lead to a more efficacious treatment of pain or opiate withdrawal syndrome in newborn infants with a decreased chance of adverse drug reactions.

NCT ID: NCT01323816 Completed - Critical Illness Clinical Trials

Differences in Care Provided in Intensive Care Units (ICUs) With Physician Versus Nurse Practitioner First Responders

Start date: March 2011
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate and compare outcomes of patients that have received care in medical intensive care units in a tertiary care facility with two different models; the traditional model including resident, pulmonary fellow and attending physician and a nontraditional model which has Nurse Practitioners as the direct care deliverer, a pulmonary fellow, and an attending.

NCT ID: NCT01309724 Completed - Hypotension Clinical Trials

Hemodynamic Optimization By Non-Invasive Determination Of Cardiac Output In Critically Ill Patients

Start date: January 2010
Phase: N/A
Study type: Interventional

Inadequate identification of and subsequent delayed therapy for patients with hypoperfusion (including hypovolemia, congestive heart failure and sepsis) is a common problem faced by physicians and intensivists caring for critically ill patients. Bedside clinical assessment is notoriously inaccurate in diagnosing complex etiologies of hemodynamic disturbances and in deciding on the appropriate therapy. Invasive techniques which are often required to guide diagnosis and therapy have significant risks associated with them, are costly, and are time consuming. New technology has been developed that allows for instantaneous, noninvasive monitoring of key hemodynamic parameters, like stroke volume, peak velocity and cardiac output. This new technology has the potential to improve recognition of the etiology of hemodynamic disturbances and assist the clinician in optimizing therapy based on changes in hemodynamic parameters. There is significant potential for this to be translated into improved outcomes in critically ill patients, but this has never been studied.

NCT ID: NCT01301274 Completed - Hyponatremia Clinical Trials

0.9% NaCl/Dextrose 5% vs 0.45% NaCl/Dextrose 5% as Maintenance Intravenous Fluids in Critically Ill Children

NaCrICh
Start date: February 2011
Phase: N/A
Study type: Interventional

The primary objective of this study is to compare the mean serum sodium after 48 hours of therapy with either 0.45% NaCl/dextrose 5% or 0.9% NaCl/dextrose 5%, in critically ill children requiring IV maintenance fluid administration.

NCT ID: NCT01293708 Completed - Critically Ill Clinical Trials

Realities, Expectations and Attitudes to Life Support Technologies in Intensive Care for Octogenarians:

Realistic 80
Start date: September 2009
Phase:
Study type: Observational

The purpose of this study is to understand the realities, expectations and attitudes of patients 80+ and their families about the use of life-sustaining technology, and to document the patient outcomes and family experiences associated with surviving and not surviving critical illness. Specifically in this project the investigators will determine the real outcomes of critical illness experienced by octogenarians.

NCT ID: NCT01287884 Completed - Clinical trials for Patients Needing Blood Gases

Correlation of Arterial Blood Gas (ABG) and Venous Blood Gas (VBG) in the Undifferentiated Critically Ill Patient

Start date: October 2010
Phase: N/A
Study type: Interventional

The primary objective of this study is to identify a correlation between the pH and pCO2 in arterial and venous blood. The secondary objectives include a correlation of pulse oximetry and arterial pO2 along with subgroup analyses of specific patient populations such as congestive heart failure, chronic obstructive pulmonary disease, diabetic ketoacidosis, pneumonia, overdose, and trauma.