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Respiratory Insufficiency clinical trials

View clinical trials related to Respiratory Insufficiency.

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NCT ID: NCT01322659 Completed - Clinical trials for Inadequate or Impaired Breathing Pattern or Ventilation

Weaning Using Noninvasive Positive Pressure Ventilation by Means of Helmet in Patients With Acute Respiratory Failure

Start date: March 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether helmet is effective as device for noninvasive positive pressure ventilation in the weaning from mechanical ventilation.

NCT ID: NCT01320384 Completed - Clinical trials for Acute Respiratory Failure

Clinical Effect of the Association of Noninvasive Ventilation and High Flow Nasal Oxygen Therapy in Resuscitation of Patients With Acute Lung Injury (FLORALI Study)

FLORALI
Start date: March 2011
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of the study is to compare, in patients with acute respiratory failure/acute lung injury the efficacy of three different methods of oxygenation to prevent endotracheal intubation : 1. conventional oxygen therapy (O2 conventional) 2. high flow nasal oxygen therapy (O2-HFN) 3. association of high flow nasal oxygen therapy with non invasive positive pressure ventilation (O2-HFN/NPPV).

NCT ID: NCT01318824 Active, not recruiting - Clinical trials for Neonatal Respiratory Failure

A Study of Bi-Level Positive Airway Pressure (BIPAP) Versus Non Invasive Positive Pressure Ventilation (NIPPV) for Neonatal Respiratory Failure

BIPAP
Start date: December 2010
Phase: Phase 3
Study type: Interventional

To research the effect of Bi-Level Positive Airway Pressure (BiPAP) for neonatal respiratory failure.

NCT ID: NCT01312948 Completed - Clinical trials for Obstructive Sleep Apnea

Study of the Usability and Efficacy of a New Pediatric CPAP Mask

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

This study will evaluate a newly developed pediatric mask (known as Pixi) on children aged 2-7 using continuous positive airway pressure (CPAP), or Non-invasive ventilation (NIV) treatment. The participants will undergo a monitored sleep study, followed by a 7 night trial of the Pixi mask in the home environment. During the study usability will be measured through questionnaires filled in by the parent and clinician. The study hypothesis is that the usability of the mask will be superior to the patient's usual mask.

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: NCT01301352 Completed - Clinical trials for Respiratory Insufficiency

Feeding Children Nasogastrically Versus Nasojejunally While Receiving Noninvasive Positive Pressure Ventilation

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

The investigators are studying whether it is safe and effective to provide enteral nutrition to critically ill children via the nasogastric route, as opposed to the nasojejunal route, while they are receiving noninvasive positive pressure ventilation.

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: NCT01286506 Terminated - Critical Illness Clinical Trials

Observational Study of Blood Pressure Measurements and Continuous Dialysis

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

Dialysis is used to control the fluid balance and metabolic state of patients with kidney disease. Control of the metabolic state, via electrolytes, can be monitored using labs that are routinely drawn from patients undergoing continuous hemodialysis. Control of fluid removal is much more difficult. This study aims to determine whether changes in the blood pressure associated with breathing correlate with or predict intolerance to fluid responsiveness with continuous dialysis. We hypothesize that a measurement of changes in blood pressure with breathing called arterial pulse pressure variation may be able to predict the ability to remove fluid during continuous renal replacement therapy.

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: NCT01280383 Withdrawn - Respiratory Failure Clinical Trials

Non-invasive Neurally Adjusted Ventilatory Assist

Start date: November 2010
Phase: Phase 1
Study type: Interventional

Neurally adjusted ventilatory assist (NAVA) is a new concept of mechanical ventilation. NAVA delivers assistance to spontaneous breathing based on the detection of the electrical activity of the diaphragm. The investigators will study the effects of non-invasive NAVA on respiratory muscle unloading critically ill patients.