Utility of Severity Scales in Clinical Practice in Children Hospitalized Due to Bronchiolitis.

ConditionBronchiolitis
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age5-24
SponsorSzpital im. Św. Jadwigi Śląskiej

About this trial

Prospective observational study of patients hospitalized with bronchiolitis. The objective of our study is to compare the accuracy of commonly used clinical scales for bronchiolitis to predict relevant outcomes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Tachypnoea (WHO definition).

Nasal flaring;

Grunting;

Use of accessory muscles;

Disqualifiers

None

Trial population

Hospitalized patients with diagnosis of bronchiolitis

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Number of participants requiring oxygen supplementation

Time frame
From admission to hospital discharge up to 2 weeks
2

Duration of oxygen supplementation

among those requiring oxygen

Time frame
From admission to hospital discharge up to 2 weeks
3

The time until the infant will be assessed as being 'fit for discharge'

which is defined as the point at which the infant will be feeding adequately (taking \>75% of their usual intake based on parents' assessment) and will have a saturation of at least 92% for 6 h on room air, while the axillary body temperature will remain

Time frame
From admission to hospital discharge up to 2 weeks
4

Worsening of clinical status, including the following

PICU admission

Time frame
From admission to hospital discharge up to 2 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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