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Respiratory Failure clinical trials

View clinical trials related to Respiratory Failure.

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NCT ID: NCT01372995 Completed - Respiratory Failure Clinical Trials

Vitamin D in Ventilated ICU Patients

R21 HL-110044
Start date: July 2011
Phase: Phase 2
Study type: Interventional

The increasing rate of hospital-acquired infection and antibiotic resistance are major causes of prolonged ICU stay and death in hospitalized patients. The enormous impact of ICU-related infection demands the need for cost-effective therapies that can be rapidly implemented to improve patient immune response to control infection. Unfortunately, little high-quality comparative effectiveness research has been performed on micronutrient treatment regimens as methods to decrease hospital-acquired infection in critically ill patients. Critically ill medical and surgical patients have an extremely high prevalence of vitamin D insufficiency. We will perform a rigorous, double-blind, randomized, controlled, pilot clinical trial in ventilator-dependent ICU patients to test the clinical/metabolic safety and efficacy of two doses of oral high-dose vitamin D3 therapy versus standard therapy (no supplemental vitamin D). The primary endpoint is to test whether high-dose regimens [either 50,000 or 100,000 international units (IU) of enteral vitamin D3 given daily for 5 consecutive days (total dose = 250,000 or 500,000 IU, respectively) increase plasma 25(OH)D concentrations into a desirable range (> 30 ng/mL).

NCT ID: NCT01370278 Completed - Clinical trials for Myocardial Infarction

Clearance Of Mucus In Stents (COMIS)

Start date: June 16, 2011
Phase: N/A
Study type: Interventional

The goal of this clinical research study is to compare the effects of sodium bicarbonate to normal saline when used for clearing mucus blockage in patients with airway stents.

NCT ID: NCT01337271 Completed - Respiratory Failure Clinical Trials

Performance of Neurally Adjusted Ventilatory Assist (NAVA) During Spontaneous Breathing Trial

Start date: May 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to compare a new mode of mechanical ventilation (NAVA, or Neurally adjusted Ventilatory assist) with a traditional mode (Pressure Support ventilation) on its the ability to detect patients ready for extubation (liberation from mechanical ventilation).

NCT ID: NCT01335932 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Ganciclovir/Valganciclovir for Prevention of CMV Reactivation in Acute Injury of the Lung and Respiratory Failure

GRAIL
Start date: March 10, 2011
Phase: Phase 2
Study type: Interventional

To evaluate whether administration of ganciclovir reduces serum IL-6 levels (i.e. reduction between baseline and 14 days post-randomization) in immunocompetent adults with severe sepsis or trauma associated respiratory failure. Primary Hypotheses: - In CMV seropositive adults with severe sepsis or trauma , pulmonary and systemic CMV reactivation amplifies and perpetuates both lung and systemic inflammation mediated through specific cytokines, and contributes to pulmonary injury and multiorgan system failure, AND - Prevention of CMV reactivation with ganciclovir decreases pulmonary and systemic inflammatory cytokines that are important in the pathogenesis of sepsis and trauma related complications.

NCT ID: NCT01306201 Completed - Respiratory Failure Clinical Trials

Novel Non-Invasive Monitoring Parameter in a Hospital Setting

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

Data collected from this study will be used to evaluate the performance of a monitoring algorithm.

NCT ID: NCT01286610 Completed - Sepsis Clinical Trials

Applicability and Safety of Vibration Therapy in Intensive Care Unit (ICU) Patients

VTICU
Start date: February 2011
Phase: N/A
Study type: Interventional

Vibration therapy is used for different indications in rehabilitation and sports medicine. So far, vibration therapy has not been investigated within the ICU setting. The investigators created this setting to show safety and applicability of vibration therapy in ICU patients. 30 patients will be stimulated by vibration therapy on two separate days during their ICU stay. Three collectives of equal size will be observed: One with patients on mechanical ventilation without signs of infection or suspected intracranial pressure problems, a second one with patients on mechanical ventilation in addition to signs of systemic inflammation but absence of suspected intracranial pressure problems, and a third one with patients on mechanical ventilation, signs of systemic inflammation in addition to presence of controlled intracranial pressure problems. Typical parameters of hemodynamic status, intracranial pressure and energy metabolism will be recorded for a defined period of time before, during and after vibration therapy itself. Vibration therapy will be combined with protocol based physiotherapy. Our aim is to show the effects of vibration therapy in ICU patients and its safe applicability. ADDITION 06th of May 2011: Additionally we will perform euglycaemic hyperinsulinemic clamp and intervention on one day of ICU stay in 20 patients. Under clamp conditions we will perform a vibration therapy (ProMedVi Vibrosphere™) on patients' legs. On top we will perform electrical muscle stimulation (schwa-medico, MUSKELaktiv™) on one ventral upper leg, randomized chosen. Measuring the local skeletal muscle metabolism will be done by microdialysis in Vastus lateralis on both sides - comparing vibration therapy and vibration therapy combined with electrical muscle stimulation.

NCT ID: NCT01284140 Completed - Critical Illness Clinical Trials

Improving the Sleep and Circadian Rhythms of Mechanically Ventilated Patients

Start date: January 2011
Phase: N/A
Study type: Interventional

The goal of this project is to determine whether the sleep and circadian rhythms of critically ill patients undergoing mechanical ventilation can be improved through practical strategies that can be employed at the bedside.

NCT ID: NCT01276652 Completed - Critical Illness Clinical Trials

Sleep and Circadian Rhythms in Mechanically Ventilated Patients

Start date: November 2001
Phase: N/A
Study type: Interventional

This study examines the feasibility of assessing sleep and circadian rhythmicity in critically ill patients undergoing mechanical ventilation. Secondarily, it will examine the feasibility of reducing subject exposure to environmental light and noise and of delivering routine care according to classical day/night routines.

NCT ID: NCT01249794 Completed - Respiratory Failure Clinical Trials

Non Invasive Ventilation After Cardiac Surgery

CPAP-CCH
Start date: September 2010
Phase: N/A
Study type: Interventional

Patients with respiratory failure following cardiac surgery are randomized to receive standard therapy versus non invasive ventilation. The hypothesis is that patients receiving non invasive ventilation will perform better than those who received standard therapy.

NCT ID: NCT01239433 Completed - Respiratory Failure Clinical Trials

Pathophysiologic Changes in the Respiratory System During Therapeutic Interventions

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

Airway pressures change during fiberoptic bronchoscopy and endotracheal suctioning. In this study pressure changes are examined in a mechanical lung model and in a population of ICU patients on mechanical ventilation.