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Critical Care clinical trials

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NCT ID: NCT01479153 Completed - Critical Care Clinical Trials

Venous Site for Central Catheterization

3SITES
Start date: October 2011
Phase: N/A
Study type: Interventional

Central venous catheters are needed in the critical care setting to administer drugs. Three sites are available to gain vascular access: subclavian, internal jugular and femoral. Each site has complications, but there is no randomized controlled study which compared the 3 sites. The investigators hypothesis is that subclavian catheterization reduces the risk of major complications compared to internal jugular or femoral.

NCT ID: NCT01168089 Completed - Critical Care Clinical Trials

Near Infrared Spectroscopy for Blood Glucose Measurement in Critical Care Settings

Start date: April 2008
Phase: N/A
Study type: Observational

Luminous Medical, the Sponsor is developing a glucose monitor for the critical care setting. The Sponsor's ultimate goal is to provide a near-continuous blood glucose monitor that automatically measures glucose. In this study, Luminous will evaluate the performance of the near-infrared measurement in blood samples collected from patients in the intensive care unit setting.

NCT ID: NCT01155648 Completed - Critical Care Clinical Trials

Pressure Support During Chest Wall Compression

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

The purpose of this study is to compare two physiotherapy techniques: chest wall compression versus chest wall compression plus increase of 10 cmH2O in inspiratory pressure.

NCT ID: NCT01057238 Completed - Critical Care Clinical Trials

Intensive Communication for Chronically Critically Ill

Start date: November 2005
Phase: N/A
Study type: Interventional

This study was a trial of a formal system of family meetings to support family decision makers of chronically critically ill patients in the intensive care unit.

NCT ID: NCT00998387 Completed - Critical Care Clinical Trials

Validation of the Korean Confusion Assessment Method for the Intensive Care Unit (CAM-ICU)

Start date: July 2008
Phase: N/A
Study type: Observational

The purpose of this study is to translate and validate the CAM-ICU for use in the Korean ICU setting.

NCT ID: NCT00852891 Completed - Critical Care Clinical Trials

Cardiorespiratory Changes in Patients Being Weaned Off Mechanical Ventilation

Start date: December 2005
Phase: N/A
Study type: Observational

The objective of this study was to analyze changes in cardiac function using Doppler echocardiogram in critical patients during weaning from mechanical ventilation using two different weaning methods (pressure support and T-tube) and to compare a subgroup of patients: success vs. failure in weaning and patients with vs. without heart disease.

NCT ID: NCT00851825 Completed - Critical Care Clinical Trials

Heart Rate Variability During Weaning From Mechanical Ventilation

Start date: March 2003
Phase: N/A
Study type: Observational

The discontinuation of mechanical ventilation (MV) and the recovery of spontaneous breathing can lead to important cardiovascular alterations due to changes in the intrathoracic pressure. The autonomic modulation assessed through heart rate variability (HRV) during weaning from MV and its impact on cardiorespiratory variables has not been well elucidated yet. To evaluate the effect of T-tube (TT) and pressure support ventilation (PSV) during weaning from MV on cardiorespiratory variables and heart rate variability.

NCT ID: NCT00851617 Completed - Clinical trials for Mechanical Ventilation

Does Threshold IMT Influence Weaning?

Start date: August 2004
Phase: N/A
Study type: Interventional

Patients under threshold IMT show better conditions to weaning from mechanical ventilation than the control group.

NCT ID: NCT00789412 Completed - Pain Clinical Trials

Surgical Stress Index as a Tool for Monitoring Analgesia and/or Sedation in Critically Ill Patients

Start date: August 2008
Phase: N/A
Study type: Observational

The hypothesis of the study is: Does the Surgical Stress Index (SSI) correlate with the Behavioral Pain Scale (BPS), the Ramsay Sedation Scale (RSS)and/or the Behavioral Pain Scale(BPV) and can therefore be used to monitor the quality of analgosedation in noncommunicative intensive care unit patients?

NCT ID: NCT00787098 Completed - Clinical trials for Mechanical Ventilation

Investigating Modes of Progressive Mobility

Start date: November 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the effects of specific activities with and without an early therapeutic mobility (ETM) protocol among patients who experience three or more days of mechanical ventilation. A second purpose is to examine staff/delivery system and patient factors that influence the initiation and progression of activity with and without an ETM protocol. The hypothesis is that ETM protocols will result in improved patient outcomes.