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Pneumonia, Aspiration clinical trials

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NCT ID: NCT02301845 Withdrawn - Clinical trials for Pneumonia, Aspiration

Validation of Aspiration Markers

Start date: February 2016
Phase: Phase 1
Study type: Interventional

This is an interventional crossover study aimed at validating diatom shells as a marker for cuff leak and microaspiration in mechanically ventilated, critically ill patients.

NCT ID: NCT02090205 Recruiting - Respiratory Failure Clinical Trials

Mechanical Ventilation During Cardiac Surgery

Start date: November 2014
Phase: N/A
Study type: Interventional

Background There is no unanimous opinion about a lung-protective strategy in cardiac surgery. Small randomized clinical and animals trials suggest that ventilation during cardio-pulmonary bypass (CPB) could be protective on the lungs. This evidence is based on surrogate end-points and most of studies are limited to elective coronary surgery. According to the available data, an optimal strategy of lung protection during CPB cannot be recommended. The purpose of the CPBVENT study is to investigate the effectiveness of different ventilation strategies during CPB on post-operative pulmonary complications. Trial design The CPBVENT study will be a single-blind, multicenter, randomized controlled trial. We are going to enroll 780 patients undergoing elective cardiac surgery with planned use of CPB, aortic cross-clamping and two lung ventilation. Patients will be randomized into three treatment groups: 1) no ventilation during CPB; 2) continuous positive airway pressure (CPAP) with positive end-expiratory pressure (PEEP) of 5 cmH2O during CPB; 3) ventilation with 5 acts/minute with tidal volume of 2-3 ml/Kg and a PEEP of 3-5 cmH2O during CPB. The primary end-point will be the incidence of a PaO2/FiO2 ratio <200 until the time of discharge from the ICU. The secondary end-points will be the incidence of post-operative pulmonary complications and 30-days mortality. Patients will be followed-up to 12 months after the date of randomization. Summary The CPBVENT Trial will determine whether different ventilation strategies during CPB will improve pulmonary outcome in patients undergoing cardiac surgery.

NCT ID: NCT02080754 Completed - Clinical trials for Aspiration Pneumonia

Sellick Interest in Rapid Sequence Induction

IRIS
Start date: February 4, 2014
Phase: Phase 3
Study type: Interventional

Lung aspiration can occur when a rapid sequence induction of anesthesia is performed (emergency and/or presence of at least one risk factor for regurgitation of stomach contents). The aim of this study is to assess the Sellick maneuver, which is recommended for patient at high risk of aspiration of gastric content during induction of general anesthesia, despite the lack of solid evidence of its efficacy and possible adverse effects The primary outcome of this non inferiority study is the incidence of lung aspiration whether this maneuver is effectively applied or sham.

NCT ID: NCT01881672 Completed - ICU Patients Clinical Trials

Syndrome and Aspiration Pneumonia in Intensive Care

SPIRE
Start date: November 2012
Phase: N/A
Study type: Observational

Inhalation is a common condition in patients with impaired their awareness requiring protection of the upper airway by endotracheal intubation. This inhalation may lead to chemical pneumonitis and/or bacterial pneumonia. Only the latter requires the administration of antibiotics. Patients developing such a bacterial pneumonia, has a mortality, duration of mechanical ventilation and length of ICU stay increased. However, the proportion of patients with such bacterial pneumonia, bacterial ecology and morbidity that are little known. The aim of this study is to determine the frequency of bacterial pneumonia in patients admitted to the ICU for coma and treated with mechanical ventilation

NCT ID: NCT01598402 Recruiting - Clinical trials for Head and Neck Cancer

Efficacy of Prophylactic Treatment With Antibiotics During Concomitant Chemoradiotherapy in Patients With Head and Neck Cancer to Prevent Aspiration Pneumonia

PANTAP
Start date: December 2011
Phase: Phase 2/Phase 3
Study type: Interventional

Patients with locally advanced head and neck cancer treated with chemo-radiotherapy have (during and shortly after this treatment) a high risk of developing pneumonia by aspiration. This pneumonia is often associated with a hospital admission and affects the quality of life. The purpose of the study, is to determine whether prophylactic antibiotics may decrease the development of pneumonia. Prophylactic antibiotics means that there are no signs of pneumonia are already

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: NCT01045902 Completed - Clinical trials for Pneumonia, Aspiration

BAY12-8039, iv/Oral Pulmonary Abscess/Aspiration Pneumonia

Start date: February 2001
Phase: Phase 3
Study type: Interventional

The purpose of this trial is to determine the efficacy and safety of Moxifloxacin in comparison to Sulbactam/Ampicillin in the treatment of pulmonary abscesses and aspiration pneumonia.

NCT ID: NCT00610324 Completed - Clinical trials for Ventilator-Associated Pneumonia

Effect of Oral Decontamination Using Chlorhexidine or Potassium Permanganate in ICU Patients

Start date: May 2004
Phase: Phase 4
Study type: Interventional

Oropharyngeal bacteria play an important role in the pathogenesis of nosocomial pneumonia in critically ill patients. Oral cleansing with chlorhexidine has been shown to decrease incidence of pneumonia in patients undergoing open heart surgery. Its role in critically ill general ICU patients is not yet proven. The present study proposes to study the effectiveness of twice-daily oral cleansing with 0.2% chlorhexidine solution on the incidence of nosocomial pneumonia in ICU patients admitted to a single intensive care unit of an Indian public hospital

NCT ID: NCT00580346 Withdrawn - Clinical trials for Aspiration Pneumonia

Dynamic Laryngotracheal Separation for Aspiration

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

People who aspirate after neurologic insults such as stroke often develop fatal pneumonia. This study examines the effects of dynamic vocal cord closure on swallowing. Implants placed over the chest wall are connected to electrodes placed around the nerve that closes the vocal cords. The patient triggers closure by flipping the switch of a coil taped over the skin covering the internal stimulator. Vocal cord motion is verified by videotaping through an endoscope, and the status of swallowing is documented radiologically by a modified barium swallow.

NCT ID: NCT00164957 Completed - Clinical trials for Aspiration Pneumonia

The Effect of Continuous Versus Enteral Pump Feeding in Aspiration in Tube Fed Patients

Start date: September 2002
Phase: N/A
Study type: Interventional

Background: Tube feeding had been found to be a cause of aspiration pneumonia. Continuous pump feeding at slower rates as compared to bolus feeding may be less associated with aspiration pneumonia. Methods: Randomized controlled trial Subjects: Patients expected to remain on tube feeding for 4 or more weeks Outcomes: 1) pneumonia, 2) mortality