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Sepsis clinical trials

View clinical trials related to Sepsis.

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NCT ID: NCT05194189 Recruiting - Sepsis Clinical Trials

Clinical Efficacy of Megadose Vitamin C in Sepsis

CEMVIS
Start date: February 8, 2022
Phase: Phase 2
Study type: Interventional

In this multicenter, randomized, single-blind, placebo-controlled clinical trial. Patients will be randomly assigned to receive Vitamin C or placebo for 4 days or until ICU discharge (whatever come first). The primary outcome is 28-day all-cause mortality.

NCT ID: NCT05190861 Recruiting - Sepsis Clinical Trials

Evaluation of Droplet Digital PCR Rapid Detection Method and Precise Diagnosis and Treatment for Suspected Sepsis

Start date: November 29, 2021
Phase: N/A
Study type: Interventional

Sepsis is a significant public health concern worldwide, with high morbidity and mortality. With regard to a targeted antimicrobial treatment strategy, the earliest possible pathogen detection is of crucial importance. Until now, culture-based detection methods represent the diagnostic gold standard, although they are characterized by numerous limitations. Culture-independent molecular diagnostic procedures may represent a promising alternative. In particular, droplet digital PCR (ddPCR) is a novel one-step PCR assay that achieves higher accuracy and sensitivity in detecting causing pathogens in patients with bloodstream infections.

NCT ID: NCT05186480 Recruiting - Sepsis Clinical Trials

Evaluation of the Effect of Immune Modulating Enteral Nutrition Formula

Start date: October 3, 2021
Phase: N/A
Study type: Interventional

The aim is to compare the efficacy and tolerability of an immune modulating enteral nutrition formula versus the regular formula on the outcomes of critically ill septic patients by assessment of clinical outcomes, immune profile, tolerability and enteral nutrition intolerance and laboratory markers

NCT ID: NCT05181696 Recruiting - Sepsis Clinical Trials

Retrospective Analysis of Chest X-ray Severity Scoring System of COVID-19 Pneumonia

RANCH-COVID
Start date: January 1, 2020
Phase:
Study type: Observational

The research will be retrospective, and will include all patients who were admitted during 2020 and 2021 in the COVID-19 ICU of University Hospital Center Osijek due to pneumonia caused by the Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The association of chest x-ray infiltrate evolution with changes in laboratory inflammatory parameters and respiratory function parameters will be examined.

NCT ID: NCT05179499 Recruiting - Sepsis Clinical Trials

Early Vasopressors in Sepsis

EVIS
Start date: October 11, 2022
Phase: Phase 3
Study type: Interventional

Sepsis is a life-threatening reaction to an infection. It happens when the immune system overreacts to an infection and starts to damage the body's tissues and organs. The aim of this research study is to compare the two different ways to treat sepsis, in the early phase of treatment immediately after the participants arrive in hospital. The standard approach is to give a salt solution fluid through a drip in the participants arm to start with, then adding in a medication that increases the blood flow to the participants vital organs (a vasopressor mediation called norepinephrine) if required. The alternative approach is to start the vasopressor medication immediately, and then add in extra salt solution fluid via a drip if required. Vasopressors work by increasing the blood pressure which allows a better blood flow to the internal organs. The investigators plan to see which approach is better and to see if they have a role in improving a patient's recovery time, reducing complications, the length of time they stay in hospital and longer term poor health. Based on research that has already been done, the investigators believe treating patients with vasopressors when they arrive in the Emergency Department, may have potential advantages over the standard fluids used today. However, the evidence is not clear and that is why this research is being done.

NCT ID: NCT05171699 Recruiting - Sepsis Clinical Trials

Effect of Electroacupuncture in Patients With Sepsis Associated Brain Injury

Start date: April 25, 2022
Phase: N/A
Study type: Interventional

To investigate the effect of electroacupuncture on patients with sepsis-associated brain injury.

NCT ID: NCT05146336 Recruiting - Sepsis Clinical Trials

CytOSorb TreatMent Of Critically Ill PatientS Registry

COSMOS
Start date: June 22, 2022
Phase:
Study type: Observational [Patient Registry]

Registry intended to provide a data repository and reporting infrastructure for the surveillance of CytoSorb device use in real-world critical care settings, and to serve as an objective, comprehensive, and scientifically-based resource to measure and improve the quality of patient care

NCT ID: NCT05143736 Recruiting - Sepsis Clinical Trials

Nasal and Gut Microbiota Combined Clinical Events Predicts the Prognosis of Septic Patients

Start date: January 10, 2022
Phase:
Study type: Observational

In this prospective, multicentered , diagnostic trial, nasal and fecal specimens will collected from patients with sepsis in two critical care units(ICU) at the enrollment day ,the third, seventh, and fourteen days after enrollment or until ICU discharge (whatever come first). Total DNA from the nasal and fecal specimens will be extracted, amplified, and sequenced to determined the characteristics of gut microbiota and nasal microbiota. Finally, the characteristics of gut microbiota and nasal microbiota combined clinical information will be used to construct a prediction model to predict the prognosis of sepsis.

NCT ID: NCT05136560 Recruiting - Sepsis Clinical Trials

Safety and Efficacy of Early Administration of Dexamethasone in High-risk Sepsis

Start date: January 15, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to investigate the safety and efficacy of early administration of two different doses of dexamethasone in high risk septic patients.

NCT ID: NCT05133310 Recruiting - Sepsis Clinical Trials

Effect of Simvastatin on Sepsis and Febrile Neutropenia in Patients With Acute Lymphoblastic Leukemia

Start date: November 19, 2021
Phase: Phase 4
Study type: Interventional

In general, the percentage of complete remissions is 85 - 90 % for acute lymphoid leukemia (ALL). In developing countries, percentages are lower secondary to higher sepsis-related mortality. Although the effect of statins on inflammatory response associated with sepsis has been demonstrated, including an effect on bacterial proliferation in patients with a state of immunosuppression, their effect has not been demonstrated so far in patients with hemato-oncological cancer.