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Sepsis clinical trials

View clinical trials related to Sepsis.

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NCT ID: NCT03841240 Enrolling by invitation - Clinical trials for Catheter-Related Infections

The Central Venous Catheter Related Complications in Critically Ill Patients

Start date: February 19, 2019
Phase:
Study type: Observational

In this prospective clinical study, the researchers investigate the incidence of catheter-related thrombosis and catheter-related infection during indwelling central venous catheterization in critically ill patients, and analyzed the risk factors for catheter-related complications and the relationship between catheter-related thrombi and catheter-related infections. The sample size is about 500.

NCT ID: NCT03146546 Enrolling by invitation - Sepsis Clinical Trials

STUDY00015328: Sepsis Endotypes

Start date: August 6, 2020
Phase:
Study type: Observational

Determine the utility of blood resistin concentrations, when combined with clinical data, for predicting sepsis phenotypes that are associated with poor clinical outcomes. We hypothesize that resistin is a biomarker which provides critical prognostic information when used in conjunction with standard clinical data, in patients with sepsis and septic shock.

NCT ID: NCT03141112 Enrolling by invitation - Severe Sepsis Clinical Trials

The Benefits of Early Initiation of Continual Renal Replacement Therapy in Patients With Severe Sepsis

Start date: August 2016
Phase: N/A
Study type: Observational

The study will evaluate the benefit of early initiation of CRRT in the initial phase of severe sepsis in patients admitted to the ICU. Primary evaluated end-point is 28-day mortality. Secondarily evaluated end-point is length of ICU-stay, length of stay in hospital, duration of mechanical ventilation. There are two groups. One group of participants with early CRRT initiation and another group with late CRRT initiation. Reference group no CRRT.

NCT ID: NCT03133910 Enrolling by invitation - Sepsis Clinical Trials

Pharmacokinetics and Pharmacodynamics of Ceftazidime in Pediatric ICU Patients

Start date: March 9, 2017
Phase: N/A
Study type: Observational

Mortality benefit has been proven with early antibiotic administration in sepsis. Antimicrobial therapy should be based on early achievement of effective drug concentrations by optimizing the pharmacokinetic/pharmacodynamics of individual drugs. Optimal dosing in the critically ill patient can be challenging with the rapidly changing physiology of sepsis during the first days of hospitalization with capillary leak, fluid overload, changes in cardiac output, and alterations renal clearance. Ceftazidime is the preferred beta-lactam for empiric treatment of sepsis at Lurie Children's Hospital because of its anti-pseudomonal and anti-enteric bacilli coverage, however, the majority of pharmacokinetic data currently published in pediatrics does not include Intensive Care Unit (ICU) patients. Adult pharmacokinetic/pharmacodynamics data suggest that critically ill adults with high level of illness severity may benefit from continuous or extended infusion beta lactam therapy to optimize the therapeutic concentration particularly for pathogens that are relatively resistant to beta-lactams. Understanding the changing pharmacokinetic/pharmacodynamics of ceftazidime with the progression of illness in the ICU may help determine if current dosing regimens are adequate to maintain appropriate drug concentrations to optimize antimicrobial treatment.

NCT ID: NCT03064100 Enrolling by invitation - Systemic Infection Clinical Trials

Pilot Evaluation of the FilmArray® Childhood Systemic Infection (CSI) Panel

Start date: March 21, 2017
Phase: N/A
Study type: Observational

The purpose of this study is to collect data to support decisions made by BioFire regarding assay development, panel composition, and intended use for the final FilmArray CSI reagent pouch. The study will utilize whole blood and/or plasma obtained from pediatric patients under 18 years of age that present with acute fever.

NCT ID: NCT03010410 Enrolling by invitation - Sepsis Clinical Trials

Platelet Immune Responses in Aging and Influenza and Sepsis (INVACS)

Start date: December 21, 2014
Phase:
Study type: Observational

Aging is associated with immunosenescence and impaired host defense mechanisms, contributing to influenza-related morbidity and mortality. Preliminary data demonstrate that the platelet transcriptome is markedly different between healthy subjects and influenza patients. Interferon-induced transmembrane proteins (IFITM) family members are among the transcripts significantly increased in platelets during influenza and expression of IFITM-3 is impaired in elderly subjects, a pattern associated with increased mortality. This study will build on these data and investigate if aging influences the expression of platelet IFITM family members in patients with influenza and sepsis. This study will prospectively determine if aging alters the induction of (IFITMs) in platelets from hospitalized influenza and sepsis patients. The study will also determine if diminished expression of IFITM family members correlates with an increased risk of adverse outcomes in older influenza and sepsis patients.

NCT ID: NCT02258984 Enrolling by invitation - Severe Sepsis Clinical Trials

Can the Venus 1000 Help Clinicians Treat Patients With Severe Sepsis or Acute Heart Failure? The CVP Trial

Start date: October 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the impact that the Venus 1000 non-invasive CVP system has on the management of emergency department (ED) patients with fluid sensitive conditions.

NCT ID: NCT02204215 Enrolling by invitation - Sepsis Clinical Trials

Electric Acupuncture for ICU-acquired Weakness in Mechanical Ventilation Patients

EA-ICUAW
Start date: January 2014
Phase: N/A
Study type: Interventional

Intensive care unit acquired weakness (ICU-AW) is common and dramatically affect recovery. The purpose of this study is to determine whether electric acupuncture therapy is effective in the treatment of ICU-AW especially in the patients receiving mechanical ventilation with sepsis or multiorgan system failure.

NCT ID: NCT01085994 Enrolling by invitation - Sepsis Clinical Trials

Procalcitonin Monitoring May Decrease Antibiotic Use in the Intensive Care Unit

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

Sepsis is common and is associated with significant mortality, morbidity and health-care costs. Unfortunately, its diagnosis is not straightforward because its signs and symptoms are neither specific nor sensitive; in addition, microbiological cultures lack specificity, sensitivity and are plagued by high turn-around times. Because the delay in the institution of antimicrobial therapy may be deleterious, broad-spectrum antibiotics are widely used in ICU-patients, even when they are not needed. Procalcitonin may not be the long sought for bio-marker to establish the diagnosis of sepsis but may help decrease the duration of the administered antibiotic courses once they are started.