Clinical Trials Logo

Respiratory Failure clinical trials

View clinical trials related to Respiratory Failure.

Filter by:

NCT ID: NCT01806532 Recruiting - Respiratory Failure Clinical Trials

Regional Lung Inflammation and Expansion in Mechanically Ventilated Patients - a PET/CT Study

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

The goal of this study is to investigate acute respiratory distress syndrome (ARDS) and septic lung with positron emission tomography (PET) imaging and to examine the distribution of inflammation, as measured by neutrophil metabolic activity.

NCT ID: NCT01797614 Recruiting - Respiratory Failure Clinical Trials

Intra-abdominal Pressures During the Spontaneous Breathing Trial

IAP_SBT
Start date: January 2012
Phase: N/A
Study type: Observational

Increased intra-abdominal pressure (IAP) affects pulmonary dynamics. However, little is studied whether pulmonary dynamics affects IAP. We hypothesize that the change of IAP can also reflect the change of pulmonary dynamics. In this study, we choose patients who received spontaneous breathing trial to answer the hypothesis.

NCT ID: NCT01777035 Completed - Respiratory Failure Clinical Trials

Early Mobilization in the ICU

Start date: July 19, 2011
Phase: N/A
Study type: Interventional

To study all ICU patients with an independent baseline functional status , who experience a critical illness requiring intubation and mechanical ventilation evaluating long-term cognitive and executive function and long term cost effectiveness in survivors who required mechanical ventilation.

NCT ID: NCT01776333 Not yet recruiting - Respiratory Failure Clinical Trials

A Randomized Controlled Trial of a Video Decision Aid in the ICU

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

Randomized Controlled Trial of a Video Decision Aid in the ICU in surrogates of admitted patients.

NCT ID: NCT01757093 Completed - Respiratory Failure Clinical Trials

Evaluation of Oxygen Consumption and Energy Expenditure During Spontaneous Breathing Trial.

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

The purpose of this study is to compare the oxygen consumption and energy expenditure during the spontaneous breathing trial.

NCT ID: NCT01751724 Terminated - Respiratory Failure Clinical Trials

Caffeine to Reduce Mechanical Ventilation in Preterm Infants

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

Most premature infants require mechanical ventilation for prolonged periods of time and a significant proportion of them develop Bronchopulmonary Dysplasia (BPD). Caffeine is a stimulant of the respiratory center and has been used for the treatment of Apnea of Prematurity in infants not requiring mechanical ventilation or to facilitate weaning from mechanical ventilation by starting therapy shortly before extubation. Recently the use of Caffeine in ventilated infants has been initiated earlier because of the reported reduction in BPD. However there is paucity of data supporting this practice. Because protracted mechanical ventilation and supplemental oxygen increase the risk of developing BPD, a therapy that would facilitate the reduction of the respiratory support and shorten its duration is desirable. Therefore, it is of importance to evaluate the effects of early Caffeine initiation and administration during the course of mechanical ventilation in preterm infants by means of a randomized placebo-controlled trial. Hypothesis: The primary hypothesis of this study is that early use of caffeine in mechanically ventilated preterm infants will reduce the time to first elective extubation and secondarily, that this will reduce the total duration of mechanical ventilation and oxygen supplementation, and reduce the incidence and severity of BPD. Objective: The objective of this trial is to evaluate the effects of early caffeine use during mechanical ventilation on the time to first elective extubation, total duration of mechanical ventilation and oxygen supplementation, and the incidence of BPD. Study Design: This will be a single-center prospective, randomized, double-blind, placebo controlled clinical trial. Population: Premature neonates born between 23 and 30 completed weeks of gestation, who require mechanical ventilation within the first 5 days of life will be enrolled. Infants with major congenital anomalies or small for gestational age will be excluded. Methods: Infants will be randomized within the first 5 days to receive a study drug consisting of either blinded Caffeine citrate or blinded Placebo (equivalent volume of normal saline). Infants will continue to receive the study drug until the first elective extubation.

NCT ID: NCT01717651 Terminated - Respiratory Failure Clinical Trials

Muscle Atrophy in Patients With Severe Sepsis

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

This study is being done to help determine whether patients with severe sepsis (overwhelming inflammation in the body as a result of an infection) lose muscle and become weak more rapidly than patients with other severe illnesses. Weakness and muscle loss that develops after a severe illness is a serious problem. Patients who develop weakness and have a decrease in muscle size often have to stay in the hospital longer and have a higher chance of dying. At the current time, it is not clear whether certain severe illnesses are more likely to cause weakness and muscle loss. This study will be done to measure the changes in muscle size and strength as a result of each patient's illness

NCT ID: NCT01705119 Active, not recruiting - Respiratory Failure Clinical Trials

The Effects of Vertical Position on Gas Exchange in Patients With Respiratory Failure

Start date: October 1, 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate how changing from a supine to upright position affects gas exchange for patients with hypoxemic respiratory failure. The research question is: will oxygen saturation and/or partial pressure of oxygen in the blood change when a patient with hypoxemic respiratory failure moves from a supine to upright position?

NCT ID: NCT01692847 Completed - Respiratory Failure Clinical Trials

Examination of the Impact of Better Surveillance and Communication of Patient Deterioration on Patient Related Outcomes

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

A hospitals manual method of patient monitoring will be implemented in an automated system and supported by an early patient deterioration detection for timely escalation. The purpose of this study is to assess if clinical outcomes of patients in Acute Care are significantly improved by such a system.

NCT ID: NCT01683526 Completed - Respiratory Failure Clinical Trials

Safety and Efficacy of Endotracheal Intubation Using Glidescope Video-Laryngoscope

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

The safety and efficacy of a video-laryngoscope as a primary intubation tool in urgent endotracheal intubation of critically-ill patients has not been well-described in the literature. This study will answer whether using a VL will impact on the efficacy and safety of intubation compared with a traditional direct laryngoscopy.