An interventional study of nasal continuous positive airway pressure in Bronchiolitis Acute Viral, Bronchiolitis and Bronchiolitis Acute, sponsored by ameer asadullah gull. Status unknown at 1 site in Pakistan. Open to participants aged 2 Months to 2 Years. Per ClinicalTrials.gov, last updated 2021-08-04.
Sponsored by ameer asadullah gull · Not applicable, Interventional, and Treatment
This study is designed to assess the effectiveness of nasal continuous positive airway pressure in reducing respiratory distress in children with bronchiolitis
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.
30 studies on the registry are indexed under Bronchiolitis, Viral; 2 are open to participants now.
This study's planned enrollment of 96 is above the median of 85 across 25 interventional studies indexed under Bronchiolitis, Viral.
Browse Bronchiolitis, Viral studies →This is the only study on the registry with ameer asadullah gull as lead sponsor.
Compared within Bronchiolitis, Viral, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Bronchiolitis. The counts are of registry records indexed under each term, refreshed daily. How we classify →
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
In this arm, oxygen inhalation will be provided without positive end expiratory pressure
In this arm, positive end expiratory pressure will be provided by nasal continuous positive airway pressure
Device: nasal continuous positive airway pressure
positive end expiratory pressure will be applied by nasal continuous positive airway pressure
reduction in seattle score
seattle score will be noted and compared for both groups
Time frame: after 12 hours
Started Sep 2020 (actual). Primary completion is estimated for Sep 2021, 11 months after the start.
How these figures are worked out, and which studies are left out of them.
This study is status unknown, as verified in Jul 2021. You cannot join it, but the record below documents what was studied.
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