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Shock clinical trials

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NCT ID: NCT01836302 Completed - Septic Shock Clinical Trials

Septic Shock and Delirium Because of rSO2 Abnormalities in Intensive Care Unit Patients (The SAD BRAIN Study)

Start date: August 2012
Phase: N/A
Study type: Observational

Delirium in the ICU is a prevalent problem occurring in up to 80% of ICU patients. A potential cause of delirium in ICU patients could be cerebral hypoxia. Septic shock is associated with high rates of delirium. The aim of this pilot study is two fold. First, to determine the feasibility and potential challenges of measuring cerebral oxygenation in ICU patients with severe sepsis and septic shock. And second, to see if the incidence and magnitude of cerebral desaturations correlated with ICU acquired delirium as measured by the Confusion Assessment Method (CAM) scores.

NCT ID: NCT01836224 Completed - Clinical trials for Cirrhosis With Septic Shock

Efficacy and Safety of Monotherapy With Noradrenaline and Terlipressin in Patients of Cirrhosis With Septic Shock Admitted to Intensive Care Unit

Start date: October 2012
Phase: N/A
Study type: Interventional

The Patient evaluated in Emergency room since admission and detailed history and clinical examination done .The in hospital cases where sepsis is the culprit and shifted to Intensive Care Unit (ICU) in view of septic shock were included since onset of shock. Initial fluid resuscitation done and if the patient were no fluid responsive they were randomized into arms noradrenaline or terlipressin and the dose escalated to achieve the primary objectives. At the same time the strict vitals monitoring and standard medical therapy for sepsis including antibiotics and other supportive therapy continued. The patients were followed up till discharge, death or up to 28days after enrollment into the protocol (whichever the longest). The detail methodology has been explained in column 14 later.

NCT ID: NCT01827007 Completed - Septic Shock Clinical Trials

Assessment of Fluid Responsiveness by Elevation of PEEP in Patients With Septic Shock

Start date: January 2008
Phase: N/A
Study type: Interventional

The aim of the study is to evaluate whether fluid responsiveness of the critically ill patient can be assessed by analysing the PEEP-induced hemodynamic effects to systolic blood pressure, pulse pressure, aortic blood flow, aortic time-velocity integral and left ventricular end diastolic area measured with transesophageal echocardiography (PEEP-test). The chances are compared to increase of CI after volume expansion (gold standard). In clinical practise, it would be especially relevant if PEEP-induced changes in arterial pressure variations could be used in evaluation of volume status and fluid responsiveness. However, as ECHO-derived variables are used in greater extent to guide the treatment with inappropriate evidence, the simultaneous registration of ECHO-derived hemodynamic measurements is essential in the study design.

NCT ID: NCT01818427 Completed - Clinical trials for Hemmorhagic Shock During Air Medical Transport

PreHospital Air Medical Plasma Trial

PAMPer
Start date: May 2014
Phase: Phase 3
Study type: Interventional

To determine the effect of the prehospital infusion during air transport of 2 units of AB plasma on 30 day mortality in patients with hemorrhagic shock as compared to conventional care.

NCT ID: NCT01800877 Completed - Hypotension Clinical Trials

Optimal VAsopressor titraTION Pilot Randomized Controlled Trial

OVATION
Start date: April 2013
Phase: N/A
Study type: Interventional

The purpose of this research study is to determine if it is better to give vasopressors to patients to maintain a higher blood pressure target versus a lower blood pressure target. This study is important because the information we find out will help us know how best to administer vasopressors in patients with shock in the ICU.

NCT ID: NCT01774214 Completed - Shock Clinical Trials

Pediatric Fast Fluid Trial 2

PFFT2
Start date: April 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine which of two commonly used methods of manual pediatric fluid resuscitation (The "Push-Pull Technique" vs. the "Disconnect-Reconnect Technique") allows for the most rapid administration of normal saline when this is urgently required.

NCT ID: NCT01760044 Completed - Sepsis Clinical Trials

Noninvasive Assessment of Tissue Perfusion Status in Critically Ill Pediatric Patients

Start date: January 2013
Phase: N/A
Study type: Interventional

Investigators are conducting research about oxygen levels in the body and whether it is possible to use a device to measure oxygen in the body's tissues noninvasively, without blood draws or a catheter (a plastic tube placed in a vein). Investigators would like to know how this device compares to standard measurements using blood from a catheter. This may help treat patients who may not be getting enough oxygen to their body.

NCT ID: NCT01753024 Completed - Diabetes Clinical Trials

Pancreatic Exocrine Insufficiency and Pancreatic Enzyme Supplementation in Critically Ill Adult Patients

Start date: January 2012
Phase:
Study type: Observational [Patient Registry]

Malnutrition is a frequent problem in critically ill patients that is associated with detrimental clinical outcomes. To provide adequate nutritional support, current studies focused mostly on the choice of delivery timing, formula selection and the route of administration, little attention was paid to malnutrition related to exocrine pancreatic insufficiency (EPI). In fact, malnutrition is also a major consequence of pancreatic exocrine insufficiency and pancreatic damage is commonly observed in critically ill patients without prior pancreatic diseases. Hence, EPI associated malnutrition should be concerned due to the high prevalence of pancreatic damage in critically ill patients. The aims of this study is to evaluate the incidence of EPI in critically ill adult patients and explore its potential risk factors. Moreover, the efficacy of pancreatic enzyme supplementation therapy on malnutrition in ICU patients with specific clinical characteristics will be investigated.

NCT ID: NCT01718613 Completed - Septic Shock Clinical Trials

Vasopressin Versus Norepinephrine for the Management of Septic Shock in Cancer Patients

VANCS II
Start date: November 2012
Phase: Phase 3
Study type: Interventional

Although arginine vasopressin has been used as an additional drug in refractory shock in worldwide clinical practice, there are no prospective studies using it as a first choice therapy in patients with cancer and septic shock. The aim of this study is assess if the use of arginine vasopressin would be more effective on treatment of septic shock in cancer patients than norepinephrine, decreasing the composite end point of mortality and organ failure in 28 days.

NCT ID: NCT01680783 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Non-Invasive Ventilation Via a Helmet Device for Patients Respiratory Failure

Start date: September 2012
Phase: N/A
Study type: Interventional

The objective of our study is to evaluate the efficacy of helmet ventilation as compared with Face mask in patients with respiratory failure.