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Bronchiolitis, Viral clinical trials

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NCT ID: NCT05899894 Completed - Clinical trials for Acute Viral Bronchiolitis

NAVA in Infants With Acute Viral Bronchiolitis: A Feasibility Study

Start date: November 5, 2019
Phase: N/A
Study type: Interventional

This exploratory intervention feasibility study aims to evaluate the use of a novel mode of ventilation known as Neurally adjusted ventilatory assist (NAVA) in infants with acute viral bronchiolitis. The main aims are: 1. To determine whether an optimal combination of NAVA support level and Positive End Expiratory Pressure (PEEP) exists that can: 1. maximise aspects of respiratory muscle unloading and 2. minimize air trapping 2. To evaluate the impact of two morphine infusion doses on comfort levels and respiratory drive (standard = 20mcg/kg/hr, low = 5mcg/kg/hr) during ventilation titration. Patients will act as their own control and will be randomly allocated to receive either standard or low dose morphine. They will receive the alternate dose on day 2. During each period of morphine dosing ventilation levels will be titrated and vital signs, respiratory parameters and comfort b scales will be recorded.

NCT ID: NCT05799677 Completed - Reflexology Clinical Trials

The Effect of Reflexology in Patients With Viral Bronchiolitis

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

To test the influence of reflexology on bronchiolitis.

NCT ID: NCT04677556 Completed - Clinical trials for Severe Viral Bronchiolitis

Work of Breathing in Bronchiolitis Under Non-invasive Ventilation

BRONCHIO-VNI
Start date: January 5, 2021
Phase: N/A
Study type: Interventional

Severe acute viral bronchiolitis is the leading cause of pediatric intensive care admission. The first-line recommended ventilation support is continuous positive airway pressure (CPAP), which reduces the work of breathing (WOB) and improves gas exchange. Although Non invasive Positive Pressure Ventilation (NiPPV) is increasingly used in case of CPAP failure to avoid intubation, no study has yet evaluated if this support could effectively reduce the effort of breathing. Our hypothesis is that NiPPV could reduce WOB more effectively than CPAP alone, and might lead to reduce intubation in the most severe bronchiolitis. The purpose of this study is to compare WOB between CPAP and NiPPV, thanks to esophageal pressure measurement, in infants hospitalized for severe acute bronchiolitis.

NCT ID: NCT03835858 Completed - Bronchiolitis Clinical Trials

Safety of Airway Clearance in Non-hospitalized Infants With Acute Viral Bronchiolitis

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

Bronchiolitis is a disease that can occur in a mild form and moderate, and often does not require hospitalization. The technique of prolonged slow expiration followed by cough caused in children not hospitalized with mild and moderate bronchiolitis can improve clinical severity

NCT ID: NCT03738501 Completed - Clinical trials for Acute Viral Bronchiolitis

Slow Expiratory Technique to Improve Alimentation in Children With Bronchiolitis

BRONCHIOL-EAT
Start date: January 2, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to determine wether a single chest physiotherapy session with slow expiratory technique (SET) improves infants with viral bronchiolitis quality of life (food intake and sleep) on the next 24 hours.

NCT ID: NCT03298217 Completed - Bronchiolitis Clinical Trials

Peak Tidal Inspiratory Flow in Infants With Moderate to Severe Acute Viral Bronchiolitis

DEBIB
Start date: November 21, 2017
Phase: N/A
Study type: Interventional

This aim of this study is to measure the peak tidal inspiratory flow (PTIF), using spirometry, in young infants with moderate to severe acute viral bronchiolitis (AVB). PTIF is important to consider for the management of AVB with High Flow Nasal Cannulae (HFNC). Indeed, efficiency with HFNC is optimal provided that the settled flow is equal or higher than the patient's PTIF. However, PTIF values in infants with AVB have never been determined.

NCT ID: NCT03062917 Completed - Respiratory Failure Clinical Trials

Nasal and Bronchial Absorption Sampling in RSV Bronchiolitis

RSV-SAM
Start date: October 2, 2015
Phase: N/A
Study type: Interventional

This study will compare the novel methods of NS and BS with the standard technique of nasophayngeal aspiration (NPA) and routine ETT suction. We shall assess the samples for diagnosis of RSV, viral load and immune responses in the airways of babies with RSV infection. We shall also assess the genetics of babies included in this study, to see if they may be vulnerable to RSV infection.

NCT ID: NCT02853838 Completed - Clinical trials for Bronchiolitis, Viral

Chest Physiotherapy in Infants Between 0 and 12 Months Old With Acute Bronchiolitis SRV(+)

Start date: March 2015
Phase: N/A
Study type: Interventional

The purpose of this research is to determine the effect of prolonged slow expiration techniques, provoked coughing and standard therapy compared to chest wall manual vibration and standard therapy in infants between 0 and 12 months old with confirmed diagnosis of acute bronchiolitis SRV (+). The effect will be measured on respiratory insufficiency and use of supplementary oxygen.

NCT ID: NCT02602678 Completed - Clinical trials for Severe Bronchiolitis

Prone Position Effects on Work of Breathing and Intrinsic PEEP in Children With Severe Acute Viral Bronchiolitis

BRONCHIO-DV
Start date: November 2015
Phase: N/A
Study type: Interventional

Acute viral bronchiolitis is the first cause of respiratory distress in infant. Airway inflammation increases the respiratory system resistances and dynamic hyperinflation. This leads to an increase in the work of breathing. In Chronic obstructive pulmonary disease patients as in neonates, prone position (PP) improves lung function and decreases the end expiratory lung volume. The investigators hypothesized that in infants with severe bronchiolitis, prone position reduces the intrinsic Positive End Expiratory Pressure (PEEPi) and the work of breathing (WOB). The investigator designed a prospective randomized crossover study with 16 infants younger than six months who need ventilatory support by nasal continuous positive airway pressure (nCPAP) for severe acute viral bronchiolitis. Work of breathing (product time pressure) and PEEPi will be estimated using an esophageal pressure probe in prone and supine position.

NCT ID: NCT02571517 Completed - Clinical trials for Bronchiolitis, Viral

Glucocorticoid Therapy Impact on the Inflammatory Response and Clinical Evolution in Patients With Severe Bronchiolitis

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

The purpose of this study is to to demonstrate that a 7-day course of systemic glucocorticoids decreases the inflammatory activity of moderate or severe bronchiolitis in paediatric patients compared to the standard treatment. To evaluate the morbidity (regarding to the clinical course: Intensive Pediatric Unit Care unit (PICU) admission, mechanical ventilation, ionotropic support, nosocomial infection, rescue therapy for respiratory failure; duration of PICU stay and hospitalization; and exitus) between the treatment and the control groups.