Nasal Bubble Continuous Positive Airway Pressure in Reducing Respiratory Distress in Children With Bronchiolitis

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

96 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-09-06

Study Completion Date

2021-09-05

Brief Summary

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This study is designed to assess the effectiveness of nasal continuous positive airway pressure in reducing respiratory distress in children with bronchiolitis

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Detailed Description

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In this study, after taking consent from caretakers, patients of brochiolitis will be randomly assigned to either a standard care group or a nasal continuous positive airway pressure group. Both groups will be followed for respiratory distress. Respiratory distress will be compared by using Seattle sore of respiratory distress.

Conditions

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Bronchiolitis Acute Viral Bronchiolitis Bronchiolitis Acute Bronchiolitis, Viral Nasal Continuous Positive Airway Pressure

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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standard care

In this arm, oxygen inhalation will be provided without positive end expiratory pressure

Group Type NO_INTERVENTION

No interventions assigned to this group

nasal continuous positive airway pressure

In this arm, positive end expiratory pressure will be provided by nasal continuous positive airway pressure

Group Type EXPERIMENTAL

nasal continuous positive airway pressure

Intervention Type DEVICE

positive end expiratory pressure will be applied by nasal continuous positive airway pressure

Interventions

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nasal continuous positive airway pressure

positive end expiratory pressure will be applied by nasal continuous positive airway pressure

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Children presenting with history of cough, and tachypnea and wheezing on clinical examination

Exclusion Criteria

* Patients needing mechanical ventilation at the time of admission
* Patients whose caretakers refuse written informed consent
* Patients having consolidation on chest X-Ray

Minimum Eligible Age

2 Months

Maximum Eligible Age

2 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No