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Critical Illness clinical trials

View clinical trials related to Critical Illness.

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NCT ID: NCT01354197 Recruiting - Critical Illness Clinical Trials

The Thai Surgical Intensive Care Study (Thai-SICU Study)

THAI-SICU
Start date: April 2011
Phase: N/A
Study type: Observational

- Overall treatment outcomes of University base SICU - Incidence of adverse events in SICU - Factor associated to adverse events in SICU

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: NCT01343316 Terminated - Critical Illness Clinical Trials

Benefits of Post-Pyloric Feeding Tubes in Critically Ill Patients

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

The purpose of this study is to determine the benefit of feeding critically-ill patients beyond the stomach (post-pyloric). Furthermore, because of the advent of two new post-pyloric feeding tubes (Tiger 2 and Syncro BlueTube) designed to improve post-pyloric placement, the investigators will be evaluating the benefits of those two tubes as well.

NCT ID: NCT01333059 Terminated - Respiratory Failure Clinical Trials

Cycling of Sedative Infusions in Critically Ill Pediatric Patients

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

The purpose of this study is to determine if the reduction of the total amount of sedative critically pediatric ill patients receive in the PICU will achieve a significant decrease in mechanical ventilation days and a decrease in the overall length of stay in the PICU and hospital.

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: NCT01317381 Recruiting - Clinical trials for Critically Ill Patients

ICG- Livertest Versus New Biomarkers as Prognostic Markers in Critically Ill ICG- Livertest Versus New Biomarkers as Prognostic Markers in Critically Ill

(Greenpep)
Start date: May 2010
Phase: Phase 4
Study type: Observational

ICG- Leberfunktionstest versus "neue" Biomarker als prognostischer Marker bei intensivmedizischen Patienten

NCT ID: NCT01311128 Terminated - Critically Ill Clinical Trials

Determination of the Accuracy of a Non-Invasive Continuous Blood Pressure Device

Start date: February 16, 2011
Phase:
Study type: Observational

This protocol will test a new non-invasive device, the T-line, in continuously determining heart rate and blood pressure in operative and critically ill patients. The accuracy of the device will be compared to the standard radial artery catheter, as well as to the non-invasive blood pressure cuff. The T-line will also be compared to the right heart catheter determining cardiac output in at least 20 patients. Hypothesis: the T-line device will determine blood pressure and heart rate as accurately as a standard radial arterial catheter and a blood pressure cuff in perioperative patients.