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Severe Sepsis clinical trials

View clinical trials related to Severe Sepsis.

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NCT ID: NCT03015454 Completed - Sepsis Clinical Trials

An Algorithm Driven Sepsis Prediction Biomarker

Start date: December 2016
Phase: N/A
Study type: Interventional

A sepsis early warning predictive algorithm, InSight, has been developed and validated on a large, diverse patient cohort. In this prospective study, the ability of InSight to predict severe sepsis patients is investigated. Specifically, InSight is compared with a well established severe sepsis detector in the UCSF electronic health record (EHR).

NCT ID: NCT02973243 Completed - Clinical trials for Myocardial Infarction

The Vital Signs to Identify, Target, and Assess Level (VITAL) Care Study III

Start date: October 5, 2016
Phase: N/A
Study type: Observational

To evaluate the effect of automated recording on frequency of recorded scores, number of automated notifications and serious events.

NCT ID: NCT02972827 Active, not recruiting - Septic Shock Clinical Trials

Monitoring Devices in Prediction of Fluid Responsiveness in Severe Sepsis and Septic Shock

Start date: May 2015
Phase: N/A
Study type: Interventional

Comparison of noninvasive cardiac output monitor (NICOM, Cheetah Medical) with Edwards FloTrac minimally-invasive cardiac output monitor in predicting fluid responsiveness in sepsis and septic shock.

NCT ID: NCT02960854 Completed - Severe Sepsis Clinical Trials

A Study of Nivolumab Safety and Pharmacokinetics in Patients With Severe Sepsis or Septic Shock.

Start date: December 7, 2016
Phase: Phase 1
Study type: Interventional

A study to evaluate the safety, tolerability and pharmacokinetics of Nivolumab in participants with severe sepsis or septic shock.

NCT ID: NCT02903082 Terminated - Severe Sepsis Clinical Trials

Following of Myeloid-derived Suppressor Cells (MDSC) in Severe Sepsis: What Relationship With Systemic Inflammatory Syndrome?

MDSC
Start date: April 2015
Phase:
Study type: Observational

Sepsis remains a major cause of death in developed countries. A better understanding of the mechanisms involved in the regulation of inflammatory and immune response of patients with severe sepsis is an important step that could open the way for new therapeutic approaches.

NCT ID: NCT02899143 Recruiting - Sepsis Clinical Trials

Short-course Antimicrobial Therapy in Sepsis

Start date: September 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the effect of a short course antimicrobial therapy (5-days) versus a 10-days therapy on sepsis-related organ dysfunction.

NCT ID: NCT02887274 Recruiting - Sepsis Clinical Trials

Application of Stimulated Immune Response Change to Predict Outcome of Patient With Severe Sepsis

SIRCSS
Start date: July 2013
Phase:
Study type: Observational

Persistence of a marked compensatory anti-inflammatory innate immune response after an insult is termed immunoparalysis. There is no biomarker available to determine the immune status of patient. Thus, the need for early and definite diagnosis of immune status of patient with sepsis, as well as the identification of patients at risk of evolving with severe organ dysfunctions, is crucial. Most important of all, speed is the key to survival. Therefore, it of crucial importance to identify which patient characteristic determines the poor prognosis. Early intervention can improve the prognosis. Investigators foresee an urgent need to identify predictors for mortality in severe sepsis, including clinical factors or immune status. Recently, the PIRO model has been proposed as a way of stratifying septic patients according to their Predisposing condition, the severity of Infection, the Response to therapy and the degree of Organ dysfunction. The immune status may be associated with above model. However, there is paucity data addressing this issue. In this study, investigators will also analyze the progression of patient condition during treatment and the associated immune status change. In the future, Investigators hope the determination of immune status may contribute to this model of classification rather than just being used as prognostic markers. Despite the advances in the knowledge of the basic processes that trigger and sustain the systemic inflammatory response in sepsis, the search for a "magic bullet" to treat this syndrome has been frustrating. The incidence of severe sepsis and septic shock still remains quite high, as does its mortality, which has decreased very little over the past decades.

NCT ID: NCT02871895 Recruiting - Sepsis Clinical Trials

Application of Biomarkers Change to Predict Outcome of Patient With Severe Sepsis

BCSS
Start date: July 2013
Phase:
Study type: Observational

In 2004, the Surviving Sepsis Campaign (SSC) introduced guidelines for the management of severe sepsis and septic shock, as well as strategies for bedside implementation. The treatment recommendations were organized in two bundles. In an international study, enrolling adult patients with severe sepsis admitted to these intensive care units, investigators found that while mortality from severe sepsis is high (44.5%), compliance with resuscitation and management bundles is generally poor in much of Asia. Investigators need to identify the patients at risk for high in-hospital mortality in order to take appropriate steps. From their past studies, investigators found that sepsis involved inflammation and coagulation. The multiple organ involvement was associated with interaction of novel biomarkers such as cytokines. There is limited data regarding comparing and application of biomarkers of different characteristic on sepsis treatment. A simultaneous detection of multiple cytokines may provide significant prognostic information. For other biomarkers, promising observation data have been put forward, but their potential needs to be evaluated in large-scale, well-designed prospective intervention studies before clinical use can be recommended. Besides many clinical studies on biomarkers were confounded by its lack of standard bundle care for severe sepsis patient. Here investigators performed a systematic study aimed at evaluating 1. the individual and combined diagnostic accuracy of biomarkers for predicting mortality; 2. whether trend change in biomarker level more useful for above prediction; 3. which biomarker or biomarker combination checked can predict patients at risk of evolving with severe organ dysfunctions.

NCT ID: NCT02820675 Completed - Sepsis Clinical Trials

Quality Improvement in Infection COntrol and Sepsis Management in MOdel Regions

icosmos
Start date: August 2015
Phase: N/A
Study type: Interventional

The German Quality Network Sepsis is an association trying to improve quality of care for patients with sepsis, severe sepsis and septic shock or being in risc thereof. The icosmos trial investigates the impact on the use of routine data, a risk adjustment algorithm and feedback to all hospitals as well as a structured implementation for regular screening for deteriorating patients, and education on in-hospital mortality.

NCT ID: NCT02794025 Completed - Severe Sepsis Clinical Trials

The Effect of Esmolol on Clinical Prognosis of Patients With Severe Sepsis

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

The purpose of this study was to investigate the effect of esmolol on hemodynamic parameters,tissue perfusion and the clinical prognosis of patients with severe sepsis