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Critically Ill clinical trials

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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: 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: NCT01168128 Completed - Critically Ill Clinical Trials

PERFormance Enhancement of the Canadian Nutrition Guidelines by a Tailored Implementation Strategy: The PERFECTIS Study

PERFECTIS
Start date: September 16, 2009
Phase: N/A
Study type: Interventional

Canadian Critical Care Nutrition Guidelines assist health practitioners in identifying best practices for feeding critically ill patients. However, guidelines have resulted in little change in Intensive Care Unit (ICU) practices, possibly because barriers to change differ between ICUs. Change may be facilitated if strategies specifically address identified barriers. The investigators hypothesize that barriers are inversely related to nutrition performance. Tailoring change strategies to overcome barriers to change will reduce the presence of these barriers and lead to improvements in nutrition practice.

NCT ID: NCT01167595 Completed - Critically Ill Clinical Trials

Enhanced Protein-Energy Provision Via the Enteral Route in Critically Ill Patients

PEPuP
Start date: September 2010
Phase: N/A
Study type: Interventional

Critically ill patients are consistently underfed. Feeding protocols are standardized system tools used to guide nutrition practices, but to date have failed to improve delivery of nutrition. The PEP uP Protocol is a new enhanced feeding protocol. Twenty North American Intensive Care Units (ICUs) will assess baseline nutrition practices. Ten ICUs will be randomized to implement the PEP uP Protocol and educational intervention, and ten will be randomized to continue usual care. Nutrition practices will be reevaluated 6 months after baseline. The investigators hypothesize that the PEP uP Protocol will increase delivery of nutrition, and may ultimately lead to improved survival of critical illness.

NCT ID: NCT01126554 Completed - Critically Ill Clinical Trials

ICG- Liver Test Versus New Biomarkers as Prognostic Markers in Critically Ill Patients

Greenpep
Start date: July 2010
Phase: N/A
Study type: Observational

Comparison of ICG liver testing with copeptin and SAPS II score as prognostic markers in critically ill patients.

NCT ID: NCT01102348 Completed - Critically Ill Clinical Trials

Enhanced Protein-Energy Provision Via the Enteral Route in Critically Ill Patients

PEP-uP
Start date: June 2008
Phase: N/A
Study type: Interventional

The purpose of this pilot study is to assess the feasibility, acceptability, and safety of a new feeding protocol, "The Enhanced Protein-Energy Provision via the Enteral Route in Critically Ill Patients: The PEP uP protocol."

NCT ID: NCT01085071 Completed - Cardiac Surgery Clinical Trials

Comparison of Two Potassium Targets Within the Normal Range in Intensive Care Patients

GRIP-COMPASS
Start date: June 2009
Phase: Phase 4
Study type: Interventional

Rationale: It is well known that distinctly abnormal blood potassium values can cause serious complications such as cardiac arrhythmias. Although potassium regulation is generally considered important, hardly any research has been done about potassium regulation in intensive care patients. The investigators hypothesize that different potassium target-values, within the as normal accepted range, may have different effects in critically ill patients. Study design: A prospective trial comparing two different potassium target-values. Potassium will be tightly regulated with the already fully operational GRIP-II computer program. Study population: 1200 adult patients admitted at the thoracic intensive care unit of the University Medical Center Groningen. Intervention: Comparison between two variations of standard therapy: potassium target-value of 4.0 mmol/L versus 4.5 mmol/L. Main study parameters/endpoints: The primary endpoint is the incidence of atrial fibrillation or atrial flutter from ICU-admission to hospital discharge. Secondary endpoints are serum levels of potassium and the other main electrolytes, renal function and renal potassium excretion, the relation with insulin and glucose, the cumulative fluid balance, (ICU) length of stay and mortality.

NCT ID: NCT01082666 Completed - Critically Ill Clinical Trials

Continuous Control of Tracheal Cuff Pressure and Microaspiration in Critically Ill Patients

Start date: October 2009
Phase: Phase 4
Study type: Interventional

We hypothesized that continuous control of tracheal cuff pressure would reduce microaspiration of gastric content as determined by pepsin level in tracheal aspirate.

NCT ID: NCT01047267 Completed - Critically Ill Clinical Trials

Pharmacokinetics of Anidulafungin on Intensive Care Unit (ICU)

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

The objective of this study is to determine whether pharmacokinetic parameters of anidulafungin correlate with disease severity and plasma protein levels in critically ill patients.

NCT ID: NCT01038622 Completed - Critically Ill Clinical Trials

Directed Immuno Nutrition by L-arginine for Critically Ill Patients

Immunolarg
Start date: November 2009
Phase: Phase 4
Study type: Interventional

The main objective of this proof-of-concept study is to demonstrate that the only administration of L-arginine, based on a suspected deficit monitored by nasal nitric oxide measurement, can improve immune functions in critically ill patients at high risk of nosocomial infection.