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Respiratory Insufficiency clinical trials

View clinical trials related to Respiratory Insufficiency.

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NCT ID: NCT01730794 Completed - Clinical trials for Acute Respiratory Failure

Neurally Adjusted Ventilatory Assist (NAVA) Study in Adults With Acute Respiratory Failure

Start date: March 28, 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to compare a specific mode of artificial ventilation (help from a breathing machine) with other modes. This specific mode is called Neurally Adjusted Ventilatory Assist (NAVA) and is different from other modes as it uses direct signals from the diaphragm (breathing muscle) to help patients breathe. The investigators believe that using these signals, NAVA can determine the exact timing for patients' spontaneous breathing effort and delivers the artificial breath at the same time (in synchrony) with their own breath. Other modes (breathing methods) may cause asynchrony between the patient and the ventilator while delivering artificial breaths because of the way they operate. Asyncrony between patient and ventilator is a risk factor for increasing the length of artificial ventilation and number of related complications. The investigators would like to find out if NAVA performs better in establishing synchrony between patient and ventilator and as a result decreasing time for artificial ventilation and increasing better outcomes.

NCT ID: NCT01726140 Recruiting - Clinical trials for Acute Respiratory Failure Requiring Reintubation

CPAP Reduces Hypoxemia After Cardiac Surgery

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

The aim of study is to evaluate whether the application of a continuous positive airway pressure (CPAP) after extubation in patients undergoing cardiac surgery can reduce hypoxemia and re-intubation rate.

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: NCT01717222 Completed - Pain, Postoperative Clinical Trials

Effect of Intraperitoneal and Intravenous Lignocaine on Pain Relief Following Laparoscopic Cholecystectomy

Start date: December 2011
Phase: Phase 4
Study type: Interventional

Laparoscopic Cholecystectomy is the treatment of choice for patients with symptomatic gall stones. For pain relief following laparoscopic cholecystectomy both intraperitoneal and intravenous administration of lignocaine has been used. But it is not clear from the existing literature which form of administration is more effective for pain relief. Hence this study has been undertaken with the following hypothesis : Intravenous lignocaine is superior to intraperitoneal lignocaine for postoperative pain relief and minimizing the stress response in laparoscopic cholecystectomy.

NCT ID: NCT01714791 Terminated - Pain Clinical Trials

Effects of Osteopathic Treatment on Pulmonary Function After Coronary Artery Bypass Graft Surgery

OSTinCARE
Start date: January 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the short and long term effects of osteopathic treatment on pulmonary function, pain and quality of life in patients after coronary artery bypass graft (CABG) surgery. The study is a randomized controlled trial.

NCT ID: NCT01713309 Completed - Clinical trials for Acute Respiratory Failure

Heparin Binding Protein in Patients With Acute Respiratory Failure Treated With GCSF (Filgrastim)

HBP-Neupogen
Start date: January 1996
Phase: Phase 2/Phase 3
Study type: Interventional

This is a study of plasma HBP -levels of a previously published trial of G-CSF in critically ill patients (Pettila et al. Critical Care Medicine 2000). The original study was a prospective, randomised, double-blind, placebo-controlled trial of filgrastim in patients with acute respiratory failure requiring intubation. In this substudy, the investigators evaluated the effect of filgrastim on HBP -concentrations in critically ill patients.

NCT ID: NCT01707303 Completed - Clinical trials for Acute Respiratory Failure

Effect Of Acute Inflammatory Mediators On Functional Limitations In Patients With Acute Respiratory Failure

Start date: July 2007
Phase: N/A
Study type: Interventional

This is a randomized, controlled, pilot study of two separate Cohorts of patients from the intensive care unit. Cohort I will enroll 50 patients and randomize to receive one physical therapy session per day or receive usual ICU care. Cohort II, will enroll an additional 50 patients and randomize to receive either two physical therapy sessions per day or usual care. Outcome will be length of hospital stay measured in days. Secondary outcomes will be mortality, ventilator days, ICU days, and for Cohort II, grip strength, dynamometer strength assessments and the short physical performance battery (SPPB). Study subjects will have blood for cytokine analysis through their first week of study.

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: NCT01693705 Not yet recruiting - Clinical trials for Respiratory Insufficiency

Outcome Evaluation of Patients After Percutaneous Tracheostomy Due to Respiratory Failure in an Intensive Care Unit

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

To determine the morbidity and mortality of patients who have undergone percutaneous tracheostomy due to respiratory failure in the critical care unit and after intensive care in the internal medicine department, including follow-up of quality of life of these patients.

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.