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NCT04989114 Clinical Trial

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

Bronchiolitis Clinical Trial

Official title:
Effectiveness of Nasal Bubble Continuous Positive Airway Pressure in Reducing Respiratory Distress in Comparison to Standard Care in Children With Bronchiolitis: A Randomized Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04989114
Other study ID # 704/RC/KEMU
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 6, 2020
Est. completion date September 5, 2021

Study information
Verified date July 2021
Source King Edward Medical University
Contact Ameer Asadullah Gull, MBBS
Phone 00923084860184
Email hellowgull@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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

Description:

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.

Recruitment information / eligibility
Status Recruiting
Enrollment 96
Est. completion date September 5, 2021
Est. primary completion date September 5, 2021
Accepts healthy volunteers No
Gender All
Age group 2 Months to 2 Years
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• nasal continuous positive airway pressure
positive end expiratory pressure will be applied by nasal continuous positive airway pressure

Locations
Country Name City State
Pakistan Mayo Hospital Lahore Punjab

Sponsors (2)
Lead Sponsor Collaborator
ameer asadullah gull King Edward Medical University

Country where clinical trial is conducted

Pakistan, 

Outcome
Type Measure Description Time frame Safety issue
Primary reduction in seattle score seattle score will be noted and compared for both groups after 12 hours
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