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Toxemia clinical trials

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NCT ID: NCT04026035 Completed - Clinical trials for Septicemia in Hemodialysis

PCR Technic Evaluation in the Microbial Diagnostic of Septicemia in Hemodialysis Patients With Catheter.

PCRDial
Start date: August 1, 2019
Phase:
Study type: Observational

The aims of this study are to evaluate the PCR on whole blood approach to determine rapidly both the susceptibility and the identification of Staphylococcus responsible of septicemia in patients under hemodialysis with catheter. The results obtained with this novel experimental approach will be compared to those obtained on the same clinical samples by the routine diagnostic laboratory.

NCT ID: NCT03996720 Completed - Sepsis Clinical Trials

Early Identification and Effective Management of Pediatric Sepsis

Start date: October 1, 2018
Phase:
Study type: Observational [Patient Registry]

In patients diagnosed as sepsis on PICU admission, early and accurate identification of patients who will develop organ dysfunction (severe sepsis) is critical for effective management and positive outcome. A multiple marker approach would improve clinical utility compared with use of a single marker. The primary goal of this part of study is to define a combination of multiple markers, derived from novel biomarkers (nCD-64, IL-27, sTREM, HLA-DR, IL-10), metabolomics and routine clinical parameters, which could predict severe sepsis and determine the severity of disease.

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: 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.

NCT ID: NCT03924518 Completed - Sepsis Clinical Trials

Adjunctive Granisetron Therapy in Patients With Sepsis or Septic Shock

GRANTISS
Start date: April 25, 2019
Phase: Phase 2
Study type: Interventional

In this prospective, single-center,randomized,controlled,single-blind clinical trial,Patients will be randomly assigned to receive granisetron or placebo for 4 days or until leaving the ICU(death or transfer from ICU to general ward or discharge). The primary outcome is all-cause death rate at 28 days.

NCT ID: NCT03923543 Completed - Sepsis Newborn Clinical Trials

Is Neutrophil to Lymphocyte Ratio a Prognostic Factor of Sepsis in Newborns With Operated Congenital Heart Disease

Start date: January 1, 2015
Phase:
Study type: Observational [Patient Registry]

The use of neutrophil lymphocyte ratio is useful for the detection of infection status in newborns after surgery