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Sepsis clinical trials

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NCT ID: NCT03974386 Completed - Septic Shock Clinical Trials

Effects of Endotoxin Absorption and Cytokine Removal Hemofilter on Severe Septic Shock

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

In recent years, many studies have pointed out that bacterial toxin and cytokine storm are the main causes of shock and multiple organ failure in patients with sepsis. Endotoxin is the main vehicle for systemic inflammatory reaction caused by gram-negative bacteria which induce sepsis. Endotoxin binds to Toll- Like receptor 4 (TLR4) trigger a cytokine storm. The amount of endotoxin is associated with shock, insufficient intestinal perfusion, and poor prognosis. Therefore, clinicians try to use various methods to antagonize the action of endotoxin, which can reduce the cytokine storm and inflammatory response to improve the prognosis of sepsis. Continuous venous venous hemofiltration plays a role in blood purification in septic shock. With different hemofiltration filters, it has different effects. By removing the inflammatory mediators caused by bacterial toxins and cytokines, shock can be improved. The study plans to receive patients with septic shock and use a hemofiltration filter that adsorbs endotoxin and removes cytokines (oXiris, Baxter Healthcare) to perform continuous venous venous hemofiltration in addition to basic septic shock resuscitation. The effect on the concentration of cytokines in the blood, the infusion dose of inotropics, the fluid balances, and the degree of organ damage was evaluated. It is hoped that the results of this pilot study can lead us to subsequent randomized clinical trials to explore whether this filter can improve the prognosis of septic shock patients.

NCT ID: NCT03960307 Completed - Sepsis Clinical Trials

Glycocalyx and Microcirculation in Sepsis

Start date: July 1, 2017
Phase:
Study type: Observational

The aim of this observative, prospective study with cross-sectional design is to explore possible correlations/associations between microcirculation parameters and sublingual endothelial glycocalyx in sepsis. Therefore, 30 critically ill septic patients and 10 healthy controls were enrolled.

NCT ID: NCT03960203 Completed - Severe Sepsis Clinical Trials

Effect of a Sepsis Prediction Algorithm on Clinical Outcomes

Start date: January 2017
Phase: N/A
Study type: Interventional

In this clinical outcomes analysis, the effect of a machine learning algorithm for severe sepsis prediction on in-hospital mortality, hospital length of stay, and 30-day readmission was evaluated.

NCT ID: NCT03952390 Completed - Sepsis Clinical Trials

Effect of Renin-Angiotensin System on Platelet in Patient With Sepsis

ERASPPWS
Start date: January 1, 2018
Phase:
Study type: Observational

As a common and serious medical condition , sepsis is a life-threatening organ dysfunction caused by a dysregulated host response to infection , which is a major and familiar cause of death in intensive care units(ICU). As a frequent laboratory abnormality in patients with sepsis , thrombocytopenia on intensive care unit admission is independently associated with increased mortality in patients. Furthermore, a low platelet count is a marker with further significance , which is always used for evaluating the prognosis of patients. Herein, this study aimed to investigate the effect of renin-angiotensin system on thrombocytopenia in patient with sepsis and explore the possible underlying molecular mechanisms.

NCT ID: NCT03943719 Completed - Septicemia Clinical Trials

Clinical Impact of the FilmArray Blood Culture Identification Panel Performed on Positive Blood Cultures From Intensive Care Patients With Septicemia

SEPSIS2016
Start date: March 1, 2017
Phase:
Study type: Observational [Patient Registry]

Molecular testing is a largely validated approach allowing rapid identification of positive blood cultures. However, due to its high cost and its limited information on susceptibility, it is considered as an add-on technique reserved for specific patient populations. In our study, we specifically evaluated molecular testing in a critical care setting and measured its impact on the therapeutic management of critically ill with positive blood cultures. Through the analysis of 110 positive blood culture episodes included in both pre- and post intervention period, we measured a drastic 14h-reduction of the time to administration of the optimal antimicrobial treatment with the use of the molecular approach.

NCT ID: NCT03938220 Completed - Sepsis Clinical Trials

Electrical Cardiometry Compared to Transthoracic Echocardiography in Fluid Responsiveness in Sepsis

Start date: June 1, 2019
Phase:
Study type: Observational

The aim of this study is to evaluate the diagnostic accuracy of electrical cardiometry (EC) for the noninvasive determination of fluid responsiveness in sepsis and agreement of (EC) compared to transthoracic echocardiography (TTE).

NCT ID: NCT03937245 Completed - Sepsis Clinical Trials

Epidemiology and Determinants of Outcomes of Hospital Acquired Blood Stream Infections in the Intensive Care

EurobactII
Start date: August 30, 2019
Phase:
Study type: Observational [Patient Registry]

Eurobact II will investigate the mortality and morbidity of hospital-acquired blood stream infections in patients treated in intensive care units (ICU). It will investigate the effects of the micro-organism and its characteristics, such as type and resistance to antibiotics on the infection and its consequences. It will also investigate the effects of the antibiotics and other treatments on survival of patients. Eurobact II will include patients from multiple ICUs in multiple countries.

NCT ID: NCT03931967 Completed - Sepsis Clinical Trials

Proadrenomedullin and Microcirculation in Monitoring Organ Dysfunction in Patient With Infection

Start date: November 8, 2018
Phase:
Study type: Observational

This study evaluates the association between plasmatic levels of Mid Regional Proadrenomedullin (MR-proADM) and the sublingual microcirculation in critical care patients admitted with infection, sepsis or septic shock.

NCT ID: NCT03926390 Completed - Clinical trials for Feeding; Difficult, Newborn

Gut Priming With Oral Bovine Colostrum for Preterm Neonates; Randomized Control Trial

Start date: September 15, 2018
Phase: N/A
Study type: Interventional

The aim was to assess the ability of bovine colostrum concentrate to reduce the incidence of late-onset sepsis episodes and necrotizing enterocolitis in artificially fed preterm neonates and its effect on T regulatory cells. And to evaluate the effect of bovine colostrum concentrate on feeding tolerance, growth, hospital stay and mortality in preterm neonates.

NCT ID: NCT03925857 Completed - Clinical trials for Organ Dysfunction Syndrome Sepsis

Prevention of Sepsis-related Organ Dysfunction With Allocetra-OTS

P-SOFA-1
Start date: January 27, 2019
Phase: Phase 1
Study type: Interventional

The trial evaluates the safety and efficacy of one and two doses of the study drug, Allocetra-OTS, in patients who have been diagnosed with sepsis.