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Shock, Septic clinical trials

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NCT ID: NCT03528213 Recruiting - Septic Shock Clinical Trials

Utility of Sodium Lactate Infusion During Septic Shock

ULIS1
Start date: October 4, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

ULIS-1 is an open-label pilot study concerning utility of molar sodium lactate in fluid balance in septic shock patients

NCT ID: NCT03497182 Completed - Sepsis Clinical Trials

Sepsis, Severe Sepsis and Septic Shock Detection by Breath Analysis

Start date: May 2, 2017
Phase: N/A
Study type: Interventional

Breath samples will be collected from patients suspected of sepsis/severe sepsis or septic shock according to hospital sepsis screening criteria in the Emergency Department.

NCT ID: NCT03475732 Completed - Sepsis Clinical Trials

Pharmacokinetics of XueBiJing in Patients With Sepsis

Start date: March 18, 2018
Phase: N/A
Study type: Interventional

Pharmacokinetics and disposition of XueBiJing compounds in patients with sepsis

NCT ID: NCT03475667 Completed - Septic Shock Clinical Trials

Comparison of Radial and Femoral Artery Site Invasive Blood Pressure Measurement in Septic Shock Patients

Start date: April 11, 2018
Phase:
Study type: Observational [Patient Registry]

Inaccurate monitoring of mean arterial pressure (MAP) could lead to improper treatment in the form of excessive fluid infusion or unnecessary vasopressor therapy; therefore, accurate hemodynamic monitoring is crucial in treatment of septic shock. In critically ill septic patients treated with vasoactive drugs, many studies reported that radial arterial pressure monitoring significantly underestimates central arterial pressure. Insertion of a femoral line allowed a substantial reduction of the infusion rate of vasoactive drugs in these patients. These findings might imply that femoral placement of arterial lines is the gold standard for invasive arterial blood pressure monitoring in shock patient. Our study aimed to determine the difference between radial (peripheral) and femoral (central) arterial pressures measured simultaneously in a group of critically ill patients receiving high dose noradrenaline therapy (≥ 0.1 mcg/kg/min).

NCT ID: NCT03472079 Recruiting - Septic Shock Clinical Trials

TIMP2*IGFBP7 and Transient AKI

BIOCHECK
Start date: May 1, 2017
Phase:
Study type: Observational

Patients with septic shock in the intensive care unit have a high risk to develop acute kidney injury (AKI) and AKI is an independent risk factor of mortality. Given the absence of validated pharmacological treatments for limiting the progression of AKI or for accelerating recovery from AKI, early intervention and the restoration of the glomerular filtration rate (GFR) in this context of septic shock might improve the patients' prognosis. One major challenge is to determine whether or not the AKI is reversible (return to normal function KDIGO 0 within 72 hours). In this retrospective study the investigators will analyze all patients admitted for a septic shock in three French ICUs between the 1st january 2014 and 01st January 2017 who developed an AKI (KDIGO ≥1) at admission and who had a determination of the urine concentration of TIMP2*IGFBP7 at admission. The investigators will determine the best threshold of TIMP2*IGFBP7 to distinguish the population of patients who will return to normal kidney function within 72 hours (KDIGO 0).

NCT ID: NCT03461900 Completed - Septic Shock Clinical Trials

Guided Fluid-balance Optimization With Mini-fluid chALlenge During Septic Shock

GOAL
Start date: June 4, 2019
Phase: N/A
Study type: Interventional

Many observational studies have highlighted an independent association between fluid overload and clinical outcomes during septic shock. To optimize fluid balance, clinician has several options to consider carefully fluid administration and avoid fluid overload. More than a general restrictive approach, a pragmatic, individual tailored approach should be considered to optimize patients' hemodynamics during acute circulatory failure. Many advances in hemodynamic monitoring were described. Mini-fluid challenge appears to be a sensible method to use for bedside assessment to optimize fluid infusion. The next step for hemodynamic management in the ICU should be to test a hemodynamic goal-directed approach to better control fluid management and eventually improve patient's outcome. The main objective of the GOAL study is to evaluate a pragmatic optimization fluid management protocol tailored to each patient's hemodynamic status based on mini-fluid challenges. This intervention will be compared to usual management based on the latest guidelines. This intervention aims to decrease organ dysfunction during septic shock. This is the first large clinical trial designed to test this hypothesis.

NCT ID: NCT03457038 Recruiting - Septic Shock Clinical Trials

Use of Fc-MBL to Detect and Monitor the Presence of PAMPs During Septic Shock

Fc-MBL/PAMPs
Start date: October 18, 2018
Phase: N/A
Study type: Interventional

Use Mannose Binding Lectin (MBL) as a biomarker to measure levels of Pathogen- Associated Molecular Patterns (PAMP) during septic shock. This will allow evaluating interest of this biomarker to monitor and manage a septic shock. Consecutive patients admitted for sepsis in Intensive Care Unit Department will be included. This biomarker will be compared to all the parameters monitored usually for these patients in standard care.

NCT ID: NCT03456180 Completed - Septic Shock Clinical Trials

Changes in Microvascular Perfusion During Blood Purification With Cytosorb® in Septic Shock

Start date: December 9, 2016
Phase: N/A
Study type: Observational

Sepsis is defined as a life-threatening event due to a dysregulated immune response to an host. Blood purification techniques may be considered as a therapeutic weapon to front sepsis and septic shock. Haemoadsorption is one of the known blood purification technique that is employed in this study, and it is based on the principle that whole blood, contacting the surface of proper designed sorbent, would be cleared of certain substrates. With haemoadsorption it is possible to de-circulate from bloodstream high molecular weight substances, such as cytokines.In this study Cytosorb® cartridge, based on haemoadsorption principle is applied on septic patients, suffering for acute kidney failure, along with continuous veno-venous haemodialysis (CVVH-D).Microcirculation has a crucial role in the natural history of sepsis. In this prospective observational non interventional study, 10 septic patients with an acute kidney failure that need CVVH are enrolled. The primary endpoint of the study is to verify an improvement in the density of microcirculatory vessels and in the quality of blood flow after exposure to Cytosorb®. These two parameters are well described synthetically by the Perfused Vessel Density (PVD). As secondary endpoints we also want to analyze the modification of microcirculation after haemoadsorption therapy: microvascular blood flow, described by the microvascular flow index (MFI) and peripheral tissue oxygen perfusion during Cytosorb® exposure using near infrared spectroscopy technique (NIRS)

NCT ID: NCT03452865 Completed - Sepsis Clinical Trials

Esomeprazole to Reduce Organ Failure in Sepsis

PPI-SEPSIS
Start date: January 28, 2020
Phase: Phase 3
Study type: Interventional

Sepsis is a severe disease with a high mortality rate and lack of efficacious therapies. Proton pump inhibitors (PPI) are drugs widely used to inhibit acid secretion by gastric cells and with a high safety profile. Carta and Rubartelli (IRCCS San Martino - Genova) have recently reported that PPI, such as esomeprazole, inhibit TNF-alfa and IL-1ß secretion. Moreover, they showed that a single administration of PPI protects mice from endotoxic shock with no adverse effects. PPI-SEPSIS is a randomized, double blind, controlled against placebo clinical trial to test if high-doses esomeprazole in septic patients reduces the severity of organs failure. In parallel, the investigators will evaluate ex vivo in monocytes from septic patients: redox state and response to inflammatory stimuli; ATP release; metabolic changes and pH; cytokine production; the effects of PPI on these parameters.

NCT ID: NCT03438097 Completed - Septic Shock Clinical Trials

Survey of Non-resuscitation Fluids in Septic Shock

SURF
Start date: March 1, 2018
Phase:
Study type: Observational

The objective of this study is to survey the type and the amount of non-resuscitation fluids that patients with septic shock receives during their first 5 days of ICU admission.