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Respiratory Aspiration clinical trials

View clinical trials related to Respiratory Aspiration.

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NCT ID: NCT01033669 Completed - Asthma Clinical Trials

Assessment Of The Inhalation Profiles Of Four Dry Powder Inhalers In Patients With Variable Degrees Of Lung Obstruction

Start date: November 2009
Phase: Phase 2
Study type: Observational

Assessment of the inhalation profiles of four dry powder inhalers in patients with variable degrees of lung obstruction

NCT ID: NCT01019525 Completed - Mouth Breathing Clinical Trials

Posture and Pulmonary Function of Mouth-breathing Children

Start date: June 2004
Phase: N/A
Study type: Observational

The purpose of this study is to characterize the posture and respiratory function of mouth-breathing children.

NCT ID: NCT01012765 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Effect of Indacaterol on Inspiratory Capacity (IC)

Start date: November 2009
Phase: Phase 3
Study type: Interventional

This study is being conducted to assess the effect of indacaterol (150 μg o.d.) on inspiratory capacity (IC), using placebo and open label tiotropium (18 μg o.d.) as comparators in patients with moderate chronic obstructive pulmonary disease (COPD). In particular, spirometric timepoints are included to elucidate the peak-IC in a period of approximately 4 hour post inhalation

NCT ID: NCT00997737 Completed - Breathing Exercises Clinical Trials

Diaphragm Activity During Incentive Spirometry and Diaphragmatic Breathing

Start date: October 2009
Phase: Phase 1
Study type: Interventional

The objective of the present study is to evaluate diaphragm activity during three breathing exercises: diaphragmatic breathing (DB), flow-oriented (Triflo II)incentive spirometry and volume-oriented (Voldyne) incentive spirometry. Seventeen healthy subjects will be studied (8 man and 9 woman).

NCT ID: NCT00997555 Completed - Pneumonia Clinical Trials

Prophylactic Bronchoscopy After Inhalation Injury in Burn Patients

Start date: October 2009
Phase: N/A
Study type: Interventional

The investigators hypothesize that the scheduled use of bronchoscopy on a regular basis after inhalation injury in burn patients will improve outcome by providing pulmonary hygiene, decrease the incidence of pneumonia, and detect pneumonia earlier than standard treatment without bronchoscopy.

NCT ID: NCT00990899 Completed - Hypertension Clinical Trials

Hypertension and Sleep Disordered Breathing in Pediatrics

Start date: October 2008
Phase:
Study type: Observational

The primary objective is to determine the prevalence of sleep disordered breathing in children with primary hypertension or pre hypertension. The secondary objectives are to determine any association factors for children with primary hypertension or prehypertension to have sleep disordered breathing be it gender, age, body mass index (BMI), family history (hx) or ethnic group.

NCT ID: NCT00962884 Withdrawn - Clinical trials for Orthostatic Hypotension

Breathing Device for Orthostatic Hypotension (OH)

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

The investigators will test whether breathing through an inspiratory resistance device will improve the ability to be upright and decrease blood pressure drops on standing in patients with orthostatic hypotension.

NCT ID: NCT00936494 Terminated - Clinical trials for Obstructive Sleep Apnea

Inferior Turbinate Reduction in Pediatric Population Failing Surgery for Sleep Disordered Breathing

Start date: June 2009
Phase: N/A
Study type: Interventional

This study will examine whether treatment of inferior turbinates in patients with continued symptoms of obstructive sleep apnea, sleep related breathing disorder, snoring, disturbed sleeping, open mouth breathing, and upper airway resistance syndrome after tonsillectomy and adenoidectomy will improve these symptoms and should be included in the treatment paradigm for treatment of sleep related breathing disorders in infants, children, and adolescents.

NCT ID: NCT00922753 Completed - Healthy Clinical Trials

Inspiratory Support Improves Preoxygenation in Healthy Subjects

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

Preoxygenation optimizes oxygen content in the functional residual capacity (FRC). Adequate preoxygenation is defined by an expiratory oxygen fraction (FEO2) > 90%. Inspiratory support and positive end expiratory pressure (PEEP) can create a better reservoir, improve gas exchange and shorten the time needed for adequate preoxygenation. The goal of the study is to evaluate the efficacy and tolerability of different levels of inspiratory support and positive end expiratory pressure during preoxygenation in healthy subjects.

NCT ID: NCT00922493 Completed - Weaning Clinical Trials

Inspiratory Muscle Training in Weaning

IMT
Start date: December 2007
Phase: Phase 4
Study type: Interventional

Background: the objective of the present inquiry was to evaluate the weaning process in intubated older people subjected to inspiratory muscle training and to correlate the predictors of ventilatory interruption with its success. Methods: the patients were divided randomly into an experimental group (EG, n=14; age=82±4 years) that received conventional physiotherapy plus inspiratory muscle training (IMT) with threshold IMT® and a control group (CG, n=14; age=81±6 years) that received only conventional physiotherapy. The predictors evaluates were the maximum inspiratory pressure (MIP) and the index of Tobin (IT). The protocol for muscle training consisted of an initial load of 30% MIP, which was increased by 10% daily; training was administered for five minutes, twice a day, seven times a week with supplemental oxygen for the entire period from the decision to wean up to extubation.