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Critical Illness clinical trials

View clinical trials related to Critical Illness.

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NCT ID: NCT01187667 Completed - Delirium Clinical Trials

Evaluation of Delirium Prevention in Critically Ill Patients

Start date: August 2010
Phase: N/A
Study type: Observational

Haloperidol is prescribed in high risk ICU patients concerning delirium (50% or more chance to develop delirium detected with the delirium prediction model PRE-DELIRIC, or patients with history of dementia or alcohol abuse)since the delirium protocol is changed and haloperidol is added as a prevention treatment we are gathering information what the effect is on several aspects of delirium

NCT ID: NCT01180894 Completed - Trauma Clinical Trials

IV Iron for the Anemia of Traumatic Critical Illness

IATCI
Start date: June 2011
Phase: N/A
Study type: Interventional

The purpose of this clinical trial is to determine whether intravenous iron supplementation of anemic, critically ill trauma patients improves anemia and reduces the need for a red blood cell transfusion.

NCT ID: NCT01179243 Completed - Critical Illness Clinical Trials

Prevalence of Microcirculatory Alterations in Intensive Care Patients

Start date: September 2011
Phase: N/A
Study type: Observational

Recent research has focused on the investigation of sublingual microcirculatory alterations in different patient categories, like cardiac surgery and sepsis. The microcirculation plays a pivotal role in tissue oxygenation and can be non invasively visualized by sidestream dark field (SDF) imaging. The objective is to carry out a international multi center study to investigate the prevalence of microcirculatory alterations in intensive care patients. Up to the present time, a comprehensive prevalence study like this has not been carried out.

NCT ID: NCT01176279 Recruiting - Critical Illness Clinical Trials

Arterial Catheter to Monitor Glycemia

CAT-GLIC
Start date: April 2008
Phase: Phase 4
Study type: Interventional

The technique of blood samples extraction from the radial artery through an arterial catheter with a 3-way stopcock and automated washing with valve of fast flow is better than the one carried out through a fixed reusable arterial blood sample syringe and its manual washing because it shows a minor incidence of the complications originated from technical manipulation as infection, pseudo-aneurysm, ischemia or thrombosis of radial artery or obstruction of the catheter. The purpose of this study is to evaluate the efficacy, in terms of adverse effects, of blood samples obtention using an arterial catheter with needless connector closed system or an arterial catheter with an arterial blood sample syringe. Also a second purpose is to compare once a day (at the same time) the values of glycose blood levels between bedside glucometer determination of arterial catheter extraction and capillar puncture, and lab determination of glycose from venous puncture, in order to determinate fluctuation in glycose levels due to peripherical hypoperfusion or to vasoactive drugs received by these in-intensive care unit patients.

NCT ID: NCT01173367 Completed - Fever Clinical Trials

Anti-pyretic Therapy in Critically Ill Adults

Start date: August 2010
Phase: Phase 2
Study type: Interventional

The impact of fever and its management in different medical and surgical populations of critically ill patients has not been explained to date. The current study aims to assess the safety and efficacy of treatment of critically ill patients with a permissive versus aggressive fever treatment strategy.

NCT ID: NCT01172132 Completed - Clinical trials for Hematological Malignancies

The Use of Intensive Care in Critically Ill Cancer Haematological Patients: "TRIAL-OH"

Start date: November 2009
Phase: N/A
Study type: Observational

The purpose of this study is to determine: - Condition of intensive care unit (ICU) admission in patients with haematological malignancies. - ICU hospital and up to one year mortality. - Assessment of post ICU burden and health related quality at 90-d and 1 year.

NCT ID: NCT01168128 Completed - Critically Ill Clinical Trials

PERFormance Enhancement of the Canadian Nutrition Guidelines by a Tailored Implementation Strategy: The PERFECTIS Study

PERFECTIS
Start date: September 16, 2009
Phase: N/A
Study type: Interventional

Canadian Critical Care Nutrition Guidelines assist health practitioners in identifying best practices for feeding critically ill patients. However, guidelines have resulted in little change in Intensive Care Unit (ICU) practices, possibly because barriers to change differ between ICUs. Change may be facilitated if strategies specifically address identified barriers. The investigators hypothesize that barriers are inversely related to nutrition performance. Tailoring change strategies to overcome barriers to change will reduce the presence of these barriers and lead to improvements in nutrition practice.

NCT ID: NCT01167595 Completed - Critically Ill Clinical Trials

Enhanced Protein-Energy Provision Via the Enteral Route in Critically Ill Patients

PEPuP
Start date: September 2010
Phase: N/A
Study type: Interventional

Critically ill patients are consistently underfed. Feeding protocols are standardized system tools used to guide nutrition practices, but to date have failed to improve delivery of nutrition. The PEP uP Protocol is a new enhanced feeding protocol. Twenty North American Intensive Care Units (ICUs) will assess baseline nutrition practices. Ten ICUs will be randomized to implement the PEP uP Protocol and educational intervention, and ten will be randomized to continue usual care. Nutrition practices will be reevaluated 6 months after baseline. The investigators hypothesize that the PEP uP Protocol will increase delivery of nutrition, and may ultimately lead to improved survival of critical illness.

NCT ID: NCT01167075 Completed - Sepsis Clinical Trials

A Study in Critically Ill Patients Investigating Tolerability and Efficacy of Low-volume Pharmaconutrition (Intestamin)

Intestamin
Start date: February 2006
Phase: N/A
Study type: Interventional

The aim of the study is to assess the efficacy and tolerability of the low-volume supplement. The investigators randomized critically ill patients to receive Intestamin plus Fresubin or Fresubin alone.

NCT ID: NCT01164449 Completed - Critical Illness Clinical Trials

Usability of Blood Glucose Control With the Space TGC System in Medical ICU Patients

DELIOS 4
Start date: July 2010
Phase: N/A
Study type: Interventional

Hyperglycemia is common in critically ill patients and associated with an adverse outcome. Thus, glycaemic control is an important issue in critical care. Despite extensive efforts of the intensive care unit staff difficulties were experienced in achieving efficient and safe glucose control. A fully automated algorithm may help to overcome some of these limitations by excluding intuitive interventions and integrating relevant clinical data in the decision-making process. Space GlucoseControl (TGC system) is a decision support system which helps to achieve safe and reliable blood glucose control in the desired ranges. Information on parenteral and enteral nutrition is automatically integrated into the calculations. The primary objective of the current study is to investigate the performance and usability of the Space TGC system for glucose control in medical ICU patients.