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Sepsis clinical trials

View clinical trials related to Sepsis.

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NCT ID: NCT04570618 Completed - Sepsis Clinical Trials

Early Prediction of Sepsis

ExPRESS
Start date: December 1, 2020
Phase: N/A
Study type: Interventional

In this clinical trial a novel Medical Device Software will be validated prospectively. The software incorporates a machine learning algorithm capable of predicting sepsis by using routine clinical variables in adult patients at Intensive Care Units.

NCT ID: NCT04567433 Completed - Sepsis Clinical Trials

Days Alive and Out of Hospital for Patients With Sepsis

Start date: September 14, 2020
Phase:
Study type: Observational

We will perform a retrospective cohort study to assess the construct validity and performance of days alive and out of hospital at day 90 (DAOH90) in cohorts of patients with sepsis and septic shock who have been included in recent clinical trials.

NCT ID: NCT04567199 Completed - Sepsis Clinical Trials

Influence of Cytosorb on Amount of Catecholamine and Mortality in Sepsis

Start date: December 1, 2018
Phase:
Study type: Observational

The aim of this retrospective study was to identify if the enrolled patient might have had a profit of Cytosorb therapy. Primarily the decline in catecholamine therapy under Cytosorb therapy will be investigated. Secondarily the outcome of surviving patients will be evaluated and compared to expected mortality due to sequential organ failure assessment (SOFA). Thirdly the patients deceased under this therapy were compared to the surviving patients.

NCT ID: NCT04553367 Completed - Septic Shock Clinical Trials

Effect of Bronchoscopy on the Outcome of Patients With Severe Sepsis With ARDS and Complicated by VAP From Prolonged Ventilation

Start date: July 2, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

to evaluate the effect of use of bronchoscopy in the course of sepsis, weaning from the ventilator, duration of ICU stays and mortality rate in septic patients with ARDS due to VAP.

NCT ID: NCT04549740 Completed - Sepsis Clinical Trials

The Role of Salivary Alpha Amylase in Sepsis

Start date: September 15, 2020
Phase:
Study type: Observational

Critical illness may be induced by different underlying life-threatening diseases, such as infection, sepsis, trauma, respiratory insufficiency or hypoxia and severe neurological status. The associated endocrine, nervous, metabolic and immunological changes are defined as acute stress syndrome. Salivary alpha-amylase is secreted from the salivary glands mainly in response to beta-adrenergic stimuli. Salivary alpha-amylase (sAA) has gained rapid popularity as a non-invasive marker of sympathetic nervous system (SNS) activity.

NCT ID: NCT04548167 Completed - Clinical trials for Bloodstream Infection (BSI)

Prolonged Cardiopulmonary Bypass Time as Predictive Factor for in Hospital Infection

Start date: September 1, 2020
Phase:
Study type: Observational

This study is to analyse the demographics and microbiological factors concerning patients undergoing cardio surgical intervention using CPB complicated with bloodstream infection (BSI) postoperatively.

NCT ID: NCT04542538 Completed - Sepsis Clinical Trials

The Impact of Premorbid Illnesses on the Risk of ICU Admission and Short-term Outcome

Start date: April 11, 2018
Phase:
Study type: Observational

The Corona virus disease 2019 (COVID-19) pandemic is currently involving all parts of the world. Several risk factors for critical illness and death from the disease have been proposed. However, it is still unclear if the observed associations between different comorbidities and chronic medications and severe COVID-19 disease and mortality is different from associations between the same factors and other severe diseases requiring intensive care unit (ICU) -care. This is important since some of the observed risk factors are very common in the aged who, by age alone, are more prone to a more severe course of any disease. By combining several registries, this study will compare, on several comorbidities such as hypertension and diabetes , the first 2000 cases of COVID-19 patients receiving critical care in Sweden to a Swedish sepsis-cohort and a Swedish adult respiratory distress syndrome (ARDS) -cohort.

NCT ID: NCT04533256 Completed - Sepsis Clinical Trials

Effects of Renal Replacement Therapy With Hemoadsoption in Patients With Sepsis

Start date: July 10, 2016
Phase:
Study type: Observational [Patient Registry]

Hemoadsorption has been demonstrated to improve clinical and paraclinical results in critically ill patients with sepsis and septic shock. The present study investigates the effects of three consecutive sessions of hemoadsorption, performed in accordance to the local protocol for treating patients with sepsis, on organ failure, severity scores and 30-days mortality. Paraclinical results and severity scores were obtained before and after the three consecutive sessions.

NCT ID: NCT04530045 Completed - Sepsis Clinical Trials

Target Attainment of TDM-guided Infusion of Piperacillin/Tazobactam and Cefepim in Critically Ill Patients

DOSATB
Start date: May 2, 2018
Phase:
Study type: Observational

Although alternative dosing strategies can improve antimicrobial exposure in critically ill patients, the high PK variability in this population means that some may still receive sub-optimal antibiotic exposure leading to unfavourable clinical outcomes. Therapeutic drug management (TDM) guided dosing is the only safe and effective way to ensure that all critically ill patients achieve therapeutic antimicrobial exposures and to minimise the likelihood of toxicity. For experts, TDM should be a standard of care, in particular for β-lactams. Nevertheless, because of the assay method for β-lactams and the need for bioanalytical experts, delays in obtaining results frequently occurred. These barriers, combined with difficulties in the interpretation of TDM results, need to be addressed in order to increase its routine utilization. Consequently, study aiming at identify which subgroup of patients or infection are more likely to benefit from TDM are urgently warranted This prospective observational study aimed at evaluating target attainment of piperacillin/tazobactam (PIP/TAZ) and cefepim (CEF) with the use of a Therapeutic Drug Monitoring (TDM) in critically patients during the routine care

NCT ID: NCT04517695 Completed - Covid19 Clinical Trials

Blood Volume Assessment in COVID-19 and Bacterial Sepsis

BVAC19
Start date: August 1, 2020
Phase:
Study type: Observational

In patients with SARS-CoV-2 or bacterial infection admitted to the intensive care unit (ICU), the state of the intravascular volume, the characteristics of the blood volume components, and the development of a vascular leak is currently unknown. The relationship of these parameters with parameters of cardiac performance, lung edema and sublingual microcirculatory perfusion parameters have never been studied.