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Critical Illness clinical trials

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NCT ID: NCT00209768 Completed - Critical Illness Clinical Trials

Use of In-Line Filtration in Critically Ill Children

Start date: February 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether the use of in-line filtration shows any effect on the outcome of sepsis, systemic inflammatory response syndrome (SIRS), thrombosis, or organ failure in critically ill children admitted to the pediatric intensive care unit (PICU).

NCT ID: NCT00207896 Completed - Critical Illness Clinical Trials

Neuroendocrine Dysfunction in Critically Ill Pediatric Patients

Start date: August 2004
Phase: N/A
Study type: Observational

Research studies in adults have shown that certain hormones may be decreased or may not work normally which contributes to how sick a person becomes. The purpose of this project is to study hormones in children. The investigators will look to see if a decrease of certain hormone levels affects how sick a child may become. This study is intended to develop a connection between hormone levels and severity of illness. It is hoped that the information gathered will help develop further studies that may more clearly explain the role of hormones in critically ill children and possibly the introduction of hormone replacement in critical illness.

NCT ID: NCT00207883 Active, not recruiting - Critical Illness Clinical Trials

Ultrasound Guided Vascular Access in Pediatric Intensive Care Patients

Start date: January 2005
Phase: N/A
Study type: Observational

The purpose of this study is to see how fast and accurate two different techniques used by physicians to insert catheters in children are. Catheters are tiny tubes which carry fluids, blood and sometimes liquid food into a person's vein. The technique currently used relies on the physical landmarks and using fingers to feel the anatomy in which to place the catheter in the vein or artery. The investigators are changing to a technique where they will use ultrasound at the patient's bedside to help physicians with placing the catheter into the blood vessel. They are comparing the use of these two methods to determine which is faster and requires fewer needle sticks.

NCT ID: NCT00205309 Completed - Critically Ill Clinical Trials

Airway IgA: Respiratory Tract IgA Levels in Critically Ill Intubated Patients

Start date: January 2003
Phase: N/A
Study type: Observational

This study will examine the impact of acute illness on sequential airway IgA levels in intensive care patients who will require prolonged intubation. Infections are the most common cause of late deaths in non-head injured trauma patients and a frequent cause of morbidity and mortality in hospitalized patients, especially intubated Intensive Care Unit (ICU) patients. Nosocomial pneumonia is the most common of these infections, and its incidence in defined populations of critically injured patients is responsive to route and type of nutrition. This study will focus on the mechanisms of specific immune mucosal defenses in intestinal and extraintestinal sites and link enteral feeding (or lack of it) with maintenance (or deterioration) of respiratory mucosal defenses.

NCT ID: NCT00202813 Completed - Clinical trials for Children in the Pediatric Intensive Care Unit or General Pediatric Care Unit Requiring a Central Venous Catheter

Study of the Use of Coated Venous Catheters in the Critically Ill Child

Start date: July 2003
Phase: Phase 4
Study type: Interventional

This study should help determine to determine whether or not the use of an antibiotic coated catheter will significantly reduce the number of central line related bloodstream infections in children requiring a CVC. This study may also determine if antibiotic coated catheters will be significantly less likely than non-antibiotic coated catheters to allow bacteria to live (colonize) in/on the catheter. The use of central venous catheters (CVC) is paramount to the care of critically ill children. Thus, in the pediatric intensive care unit (PICU), these catheters are widely used in situations when more than peripheral venous access is necessary. This central access allows the delivery of fluids, e.g, blood, medications, etc. as well as serves as a means to withdraw blood. It has been estimated that more than 250,000 nosocomial bloodstream infections occur each year, with 90% of these associated with the use of CVCs. More recently, the National Nosocomial Infection Surveillance System (NNIS) reported during 1992-2001 CVC-associated bloodstream infections (BSI) in ICU settings occurred at rates of 2.9-11.3 BSI per 1,000 catheter days. The cost of treating CVC related BSI has been estimated to be in excess of $28,000 per catheter. In the adult medical literature, there is strong evidence supporting use of antiseptic or antibiotic coated catheters to reduce the cost of hospitalization for CVC related infections. Cost-benefit studies have suggested that if the baseline incidence of CVC BSI is >0.4 BSI per 1000 catheter days, $59,000 will be saved, 7 cases of BSI will be avoided, and 1 death prevented for every 300 anti-septic impregnated CVCs used.

NCT ID: NCT00187824 Recruiting - Sepsis Clinical Trials

Regulation of Endocrine, Metabolic, Immune and Bioenergetic Responses in Sepsis

Start date: July 2004
Phase: N/A
Study type: Observational

The hypothesis of this study is that bioenergetic failure in human sepsis, related to endocrine, metabolic and mitochondrial dysfunction, is a major determinant of defective host immune responses, increasing disease severity and risk of death. The objectives of this study are to examine the relationship between the severity of illness, and temporal changes in the activity of endocrine, metabolic and bioenergetic pathways, and consequent immune dysfunction in critically ill patients with sepsis and multiple organ failure in the Intensive Care Unit.

NCT ID: NCT00182364 Completed - Critically Ill Clinical Trials

PROphylaxis for ThromboEmbolism in Critical Care Trial (PROTECT Pilot)

Start date: February 2003
Phase: Phase 3
Study type: Interventional

PROTECT Pilot objective is to assess: 1) the feasibility of timely enrollment and complete, blinded study drug administration, 2) the bioaccumulation of LMWH in patients with acquired renal insufficiency and its association with bleeding, 3) the feasibility of scheduled twice weekly lower limb ultrasounds, and 4) recruitment rates for a future randomized trial.

NCT ID: NCT00182143 Completed - Critical Illness Clinical Trials

PROphylaxis for ThromboEmbolism in Critical Care Trial (PROTECT)

Start date: May 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the effect of Low Molecular Weight Heparin (LMWH) (Fragmin, dalteparin) versus Unfractionated Heparin (UFH) on the primary outcome of proximal leg Deep Vein Thrombosis (DVT) diagnosed by compression ultrasound, and the secondary outcomes of Pulmonary Embolism (PE), bleeding, Heparin-Induced Thrombocytopenia (HIT), and objectively confirmed venous thrombosis at any site.

NCT ID: NCT00179166 Terminated - Acute Renal Failure Clinical Trials

Assessment of Metabolic Response in Critically Ill Patients With Acute Renal Failure

Start date: June 2004
Phase: Phase 2
Study type: Interventional

We hypothesize that a nutritional supplementation with higher than standard protein content (2.0 gm/Kg/day vs 1.4 gm/Kg/day) will result in improved whole-body net protein balance when administered to critically ill patients with acute renal failure (ARF).

NCT ID: NCT00178581 Terminated - Critical Illness Clinical Trials

Enteral Glutamine Supplementation for the Patient With Major Torso Trauma

Start date: June 2005
Phase: Phase 1
Study type: Interventional

Glutamine is considered a conditionally essential amino acid during critical illness. After severe trauma, glutamine supplementation into the gastrointestinal tract may help maintain bowel function. We hypothesize that for the major torso trauma patient, high dose glutamine given enterally during resuscitation from shock and continued during enteral nutrition support is absorbed, available systemically and preserves gut integrity.