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Multiple Organ Failure clinical trials

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NCT ID: NCT01465711 Completed - Sepsis Clinical Trials

The Value of PSP in Predicting Outcome in ICU Surgical Peritonitis Patients

Start date: July 2007
Phase: N/A
Study type: Observational

The purpose of this study is to determine the diagnostic accuracy of Pancreatic Stone Protein (PSP) in predicting patient outcomes with suspected peritonitis in the Intensive Care Unit after abdominal surgery and compare PPS with other blood parameters, including C-Reactive Protein (CRP), White Cell Count (WCC), Interleucin-6 (IL-6) and Procalcitonin (PCT).

NCT ID: NCT01423864 Completed - Clinical trials for Multiple Organ Failure

Intrapleural Methylprednisolone Injection for Multiple Organ Failure With Acute Respiratory Distress Syndrome

IP steroid
Start date: June 2005
Phase: Phase 2
Study type: Interventional

Acute respiratory distress syndrome (ARDS) in combination with multi-organ dysfunction syndrome (MODS) is a life-threatening condition, particularly when treatment modalities such as extracorporeal membrane oxygenation (ECMO) and catecholamine administration have failed to treat the severe condition. In this study, the investigators report patients who responded to intrapleural steroid instillation (IPSI) while being unresponsive to conventional treatment (use of intravenous steroids, nitric oxide inhalation, high-frequency oscillatory ventilation, or ECMO) for treatment of critical illnesses such as ARDS in combination with MODS.

NCT ID: NCT01367223 Completed - Clinical trials for Inflammatory Response

Modulation of Systemic Inflammatory Response in Critically Ill Children After Glutamine Supplementation

Start date: April 2010
Phase: Phase 4
Study type: Interventional

This study aims to describe the use of glutamine supplementation in the modulation of inflammatory response in critically ill pediatric patients and to determine if this decrease leads to clinical improvement in morbidity and mortality in these patients. Thus, these patients' diet could be supplemented with glutamine in order to improve their evolution. Hypothesis: From the data obtained in the study of the literature the investigators consider that: Critically ill patients have a deficit of glutamine either because of an increase in its consumption or a decrease in its availability, and therefore blood glutamine levels are low. Critically ill patients have elevated blood levels of pro-inflammatory substances (IL-6). In these patients tissue lesion inhibitors (HSP-70) in the blood are decreased. The administration of glutamine supplements to these patients decreases oxidative stress due to the increase in HSP-70. Inflammation inhibitory substances (IL-10) in the blood are decreased in these patients. The administration of glutamine supplements in these patients increase IL-10 levels. Glutamine supplements decrease the inflammatory response with a decrease in IL-6 levels.

NCT ID: NCT00965328 Completed - Acute Renal Failure Clinical Trials

Nadroparin Anticoagulation for Continuous Venovenous Hemofiltration

Start date: February 2007
Phase: Phase 4
Study type: Interventional

The low molecular weight heparin nadroparin is used for anticoagulation of the extracorporeal hemofiltration circuit. Continuous hemofiltration is a renal replacement modality for intensive care patients with acute renal failure. Up to now it is not known whether nadroparin is removed by hemofiltration or not. Accumulation would increase the risk of bleeding. Aim of the present study is to determine 1. whether nadroparin accumulates in plasma 2. whether nadroparin is removed by filtration and whether removal depends on hemofiltration dose 3. the effects of nadroparin during critical illness on coagulation and anticoagulation

NCT ID: NCT00736827 Completed - Sepsis Clinical Trials

BK Virus and Renal Dysfunction in Postoperative/Posttraumatic Critically Ill Patients

BICUK
Start date: August 2008
Phase: N/A
Study type: Observational

The purpose of this study is to find out whether acute renal failure is associated with BK virus reactivation in postoperative/posttraumatic critically ill patients with severe SIRS/sepsis and shock.

NCT ID: NCT00736723 Completed - Sepsis Clinical Trials

NT-proBNP in ICU Postoperative/Posttraumatic Patients With Shock

NICUPS
Start date: August 2008
Phase: N/A
Study type: Observational

The purpose of this study is to determine the course of NT-proBNP plasma concentrations in the context of confounding parameters in postoperative/posttraumatic critically ill patients with severe SIRS/sepsis and shock.

NCT ID: NCT00430859 Completed - Sepsis Clinical Trials

Bovine Intestinal Alkaline Phosphatase for the Treatment of Patients With Sepsis

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

Eligible patients will receive either AP or matching placebo in a double blind, randomized design and following a 2:1 ratio. All medication will be given in addition to standard care for sepsis patients. Patients will be followed for 28 days after the start of study medication administration. A blinded safety review of the study results will take place after the inclusion of 12 patients in the study.

NCT ID: NCT00271752 Completed - Sepsis Clinical Trials

The Procalcitonin and Survival Study

PASS
Start date: January 2006
Phase: N/A
Study type: Interventional

This is a randomised, single blinded, multicentre trial to evaluate whether daily procalcitonin (PCT) measurements and immediate diagnostic and therapeutic responses to abnormal values and day-to-day changes can reduce the mortality of critically ill patients in the Intensive Care Unit (ICU).

NCT ID: NCT00257244 Completed - Trauma Clinical Trials

Inflammation and the Host Response to Injury (Burns)

Start date: April 2004
Phase:
Study type: Observational

The purpose of this study is to help improve our understanding of the biology involved in the body's response to serious trauma or burn injury. The host response to trauma and burns is a collection of physiological and pathophysiological processes that depend critically upon the regulation of the human innate immune system, with particular emphasis on the inflammatory component of that system. No single research center or small group of centers has the capacity to delineate the integrated response of this complex biological system, which involves multiple molecular and genetic interactions that vary in time. Our proposal promotes the identification of important dynamic relationships that regulate the integration of this complex biological system, with the expectation that this understanding will ultimately impact the diagnosis, prognosis, and treatment of the hospitalized, severely injured patient.

NCT ID: NCT00257231 Completed - Trauma Clinical Trials

Inflammation and the Host Response to Injury (Trauma)

Start date: November 2003
Phase:
Study type: Observational

The purpose of this study is to help improve our understanding of the biology involved in the body's response to serious trauma or burn injury. The host response to trauma and burns is a collection of physiological and pathophysiological processes that depend critically upon the regulation of the human innate immune system, with particular emphasis on the inflammatory component of that system. No single research center or small group of centers has the capacity to delineate the integrated response of this complex biological system, which involves multiple molecular and genetic interactions that vary in time. Our proposal promotes the identification of important dynamic relationships that regulate the integration of this complex biological system, with the expectation that this understanding will ultimately impact the diagnosis, prognosis, and treatment of the hospitalized, severely injured patient.