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Toxemia clinical trials

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NCT ID: NCT03280147 Completed - Recurrence Clinical Trials

7 Days Versus 14 Days of Antibiotics for Neonatal Sepsis

Start date: January 1, 2019
Phase: Phase 3
Study type: Interventional

The optimum duration of intravenous antibiotic therapy for culture-proven neonatal bacterial sepsis is not known. Current practices, ranging from 7 days to 14 days of antibiotics, are not evidence-based. This is a randomized, active -controlled, multi-centric, non-inferiority trial to compare the efficacy of a 7-day course of intravenous antibiotics versus a 14-day course among neonates weighing > 1000 g at birth with culture-proven bacterial sepsis that is uncomplicated by meningitis, bone or joint infections deep-seated abscesses. The primary outcome measure is a definite or probable relapse within 21 days after stoppage of antibiotics.

NCT ID: NCT03277677 Completed - Sepsis Clinical Trials

The Effect of Fluid Resuscitation With 0.9% Sodium Chloride Versus Balanced Crystalloid Solution on Renal Function of Sepsis Patients

Start date: July 1, 2017
Phase: Phase 3
Study type: Interventional

The high chloride content of 0.9%sodium chloride (0.9%NaCl) leads to adverse pathophysiological effects in both animals and healthy human volunteers. Small randomized trials confirm that the hyperchloremic acidosis induced by 0.9%NaCl also occurs in patients. A strong signal is emerging from recent large propensity-matched and cohort studies for the adverse effects that 0.9% NaCl has on the clinical outcome in surgical and critically ill patients when compared with balanced crystalloids. Major complications are the increased incidences of acute kidney injury and the need for renal replacement therapy, and that pathological hyperchloremia may increase postoperative mortality. Fluid resuscitation with 0.9% NaCl in animals with sepsis resulted in hyperchloremic metabolic acidosis, worsened AKI, and increased mortality when compared with resuscitation with a balanced crystalloid solution. Furthermore, hyperchloremic acidosis also resulted in increased concentrations of circulating inflammatory mediators in an experimental model of severe sepsis in rats, with a dose-dependent increase in circulating interleukin-6, tumor necrosis factor-a, and interleukin-10 concentrations with increasing acidosis. Thus, in this study, investigators compared the effects of a balanced crystalloid solution with 0.9% NaCl on the renal function in severe sepsis/septic shock patients. Investigators hypothesized that balanced crystalloid solution resuscitation would decrease AKI incidence and severity and would improve immunomodulatory effect when compared with 0.9% NaCl resuscitation.

NCT ID: NCT03275090 Completed - Sepsis Newborn Clinical Trials

The Effects of Two Different Intravenous Lipid Emulsions on the Outcomes of Preterm Infants With Sepsis

Start date: February 1, 2016
Phase: Phase 4
Study type: Interventional

Introduction and objectives: Lipid emulsions play an important role in parenteral nutrition in preterm infants. We aim to evaluate the effect of two different intravenous lipid emulsions on the outcomes of neonatal sepsis in preterm infants. Methods: A randomized controlled trial is conducted in the Neonatal Care Unit of Mansoura University Children's Hospital, Egypt. Forty preterm infants with clinically suspected sepsis are enrolled and assigned randomly into one of two groups, one receive MOFS lipid emulsion (MOFS group) and the other receive pure soyabean oil-based emulsion (S group). Clinical and epidemiological data are collected. Assessment is done on 1st day and 7th day post randomization including growth parameters, complete blood count, C-reactive protein, random blood glucose, serum creatinine, serum triglyceride, soluble intercellular adhesion molecule 1 (sICAM-1) and leukocyte integrin β2. Between-groups and within-group differences will be analyzed statistically.

NCT ID: NCT03258684 Completed - Sepsis Clinical Trials

Hydrocortisone, Vitamin C, and Thiamine for the Treatment of Sepsis and Septic Shock

HYVCTTSSS
Start date: September 25, 2017
Phase: N/A
Study type: Interventional

In this prospective clinical study, the investigators compare the outcome and clinical course of consecutive septic participants treated with intravenous vitamin C, hydrocortisone, and thiamine (treatment group) with a control group treated in the investigators' ICU. The primary outcome is hospital survival. A propensity score is generated to adjust the primary outcome.There is 70 participants in each group.

NCT ID: NCT03249597 Completed - Sepsis Clinical Trials

Predict Sepsis; the Predictive Value of Bedside Measures in the Ambulance

Start date: April 3, 2017
Phase:
Study type: Observational

Sepsis is a condition with a high mortality. Septic patients are frequently difficult to identify because of their non-specific presentations. There is also a low sensitivity of clinical judgment among health care personnel, and of existing screening tools, which are in turn typically based on vital parameters. Despite prior research, no unique sepsis biomarker has been identified so far. There is a need for new strategies to identify sepsis which do not rely on vital parameters and traditional laboratory blood tests alone. The hypothesis of the investigators is that a combination of clinical variables measurable in the ambulance can be used to predict sepsis. The aim of the current study is to determine the predictive value of keywords related to symptom presentation, vital parameters and point-of-care (POC) blood tests, alone and in combination, with respect to the outcome sepsis. The study is performed in the Stockholm ambulance setting from April 2017. A total of 956 adult non-trauma patients will be included.

NCT ID: NCT03249246 Completed - Sepsis Clinical Trials

Epidemiology of Sepsis in Turkish ICUs.

Start date: January 27, 2016
Phase: N/A
Study type: Observational

The prevalence and mortality of sepsis in Turkey is not know at large. Turkish Society of Intensive Care Medicine, Sepsis Study Group conducted a multi-centre,point prevalence survey to determine the prevalence, causative micro-organisms and outcome of sepsis in Turkish ICUs.

NCT ID: NCT03246893 Completed - Septic Shock Clinical Trials

Efficacy of HFNC Versus NIV for Prevent Reintubation in Sepsis Patients

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

Post extubation respiratory failure occur in 30% of extubated patients. More than 50% of them required reintubation. Noninvasive positive pressure ventilation (NIV) had been reported as an effective tool to prevent post extubation respiratory failure. Recently, high flow oxygen nasal cannula (HFNC) had been successfully used to prevent post extubation respiratory failure and prevent reintubation in comparable with NIV among post cardiothoracic surgery and high risk for reintubated patients. There was no information about HFNC versus NIV in prevention of reintubation among severe sepsis or septic shock patients.

NCT ID: NCT03238742 Completed - Sepsis Clinical Trials

The Efficacy of Xuebijing Injection on Sepsis

Start date: October 20, 2017
Phase: Phase 4
Study type: Interventional

The Efficacy of Xuebijing Injection in Adult Patients with Sepsis

NCT ID: NCT03237728 Completed - Sepsis Clinical Trials

Study of Multiple-dose Kukoamine B Mesilate in Sepsis Patients

Start date: July 28, 2017
Phase: Phase 1
Study type: Interventional

Phase I study of multiple-dose Kukoamine B Mesilate in Sepsis Patients

NCT ID: NCT03235193 Completed - Sepsis Clinical Trials

Predictive algoRithm for EValuation and Intervention in SEpsis

PREVISE
Start date: July 1, 2017
Phase: N/A
Study type: Interventional

In this prospective study, the ability of a machine learning algorithm to predict sepsis and influence clinical outcomes, will be investigated at Cabell Huntington Hospital (CHH).