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Sepsis clinical trials

View clinical trials related to Sepsis.

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NCT ID: NCT00472628 Withdrawn - Sepsis Clinical Trials

Multi-marker INDex for the Risk Assessment of Sepsis in the Emergency departmenT (MINDSET)

MINDSET
Start date: May 2007
Phase: N/A
Study type: Observational

The purpose of the study is to procure blood samples from patients ≥18 years of age who present to the Emergency Department (ED) with at least two of the diagnostic criteria for sepsis. Samples obtained upon enrollment will be used for future testing of the Triage Sepsis Panel and other biomarkers.

NCT ID: NCT00368381 Withdrawn - Sepsis Clinical Trials

Hydrocortisone Versus Hydrocortisone Plus Fludrocortisone for the Treatment of Adrenal Insufficiency in Severe Sepsis

Start date: September 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if the combination of hydrocortisone plus fludrocortisone is more efficacious than hydrocortisone alone in treating adrenal insufficiency in severe sepsis.

NCT ID: NCT00304772 Withdrawn - Sepsis Clinical Trials

Fluconazole Versus Micafungin for Candida Bloodstream Infection in Non-Neutropenic Patients

Start date: August 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to verify the equivalence in clinical efficacy of fluconazole and micafungin for the treatment of Candida bloodstream infection in non-neutropenic patients.

NCT ID: NCT00247468 Withdrawn - Sepsis Clinical Trials

Strict Glucose Control of Pediatric Intensive Care Unit (ICU) Patients

Start date: December 2004
Phase: N/A
Study type: Interventional

The study objective is to improve morbidity and mortality of high-risk critically ill children. Our hypothesis is that a strict ICU glucose control protocol will decrease morbidity and mortality associated with hyperglycemia in a population of high-risk critically ill pediatric patients.

NCT ID: NCT00194974 Withdrawn - Hypertension Clinical Trials

Treatment Targets for Chronic Hypertension in Pregnancy

Start date: July 2004
Phase: Phase 1/Phase 2
Study type: Interventional

This project is a clinical study of women with high blood pressure who become pregnant. Preeclampsia is a syndrome developing at the end of a pregnancy characterized by an abrupt rise in blood pressure (BP), blood clotting and kidney dysfunction, and may result in premature delivery, infant death, and maternal bleeding, kidney failure and stroke. The goal is to determine whether lowering blood pressure to a normal pressure of 120/80 is associated with a lower incidence of preeclampsia. Women who are completely healthy have a 5% chance of developing preeclampsia, however women with preexisting high blood pressure have a 25% chance of this complication. Several studies, including our own suggest that higher blood pressure early in pregnancy (<20 weeks) is associated with an even higher risk of preeclampsia. Currently we, the researchers at Weill Medical College of Cornell University, do not know how to treat women with high blood pressure and/or kidney disease during pregnancy. Keeping the BP in the normal range may be beneficial to the mother. On the other hand, we are not sure if the blood pressure lowering or the medications may or may not have adverse effects for the baby. Different trials to answer this question have been performed with no clear conclusions. Because of these uncertainties, we propose to compare two different strategies for treating women with high BP who become pregnant. We will treat half the women with BP medications to normalize BP (120-130/80 mm Hg) (experimental group) and the other half with the goal of keeping the BP slightly higher (140-150/90-100 mm Hg)(standard therapy group). We will determine which approach results in healthier pregnancies, and lower incidence of preeclampsia. Reducing the incidence of preeclampsia would be of significant benefit to both mothers and babies.