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Breathe Easy Early Study (BEES): A randomised control study assessing the efficacy of early intervention with humidified high flow nasal cannula in the emergency department-Optimising outcomes in the Golden Hour of Respiratory failure.

Phase 2
Conditions
Respiratory illnesses
Chronic respiratory conditions
Congestive Heart Failure
Acute Respiratory illnesses
Cardiovascular - Other cardiovascular diseases
Respiratory - Other respiratory disorders / diseases
Registration Number
ACTRN12616000587404
Lead Sponsor
Ipswich Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
268
Inclusion Criteria

18 years and over
Symptomatic breathlessness- increased respiratory rate > 25 breaths per min and observed increased work of breathing.
Patients requiring oxygen supplementation to maintain Sp02 > 94% for acutely unwell patient OR 88% to 92% for those at risk of hypercapnic respiratory failure (in line with recruiting site hospital).

Exclusion Criteria

Recent ENT surgery
Epistaxis/ nasal trauma/ sinus problems
Altered level of consciousness
Pregnancy
Non invasive ventilation at point of triage
Pneumothorax/chest trauma
History of trauma eg. post fall
Falling GCS or GCS <9

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary outcome will be the proportion of patients who experience relief of dyspnea. This will be defined as a reduction of 20 points on a 100mm visual analogue scale (VAS), reduction in heart and respiratory rate prior to discharge from ED. The proportion of patients who achieve dyspnea relief in each group will be reported and the differences between each group (with a 95% confidence interval of the difference) will be reported.[Baseline visual analogue scale( VAS) - Included as part of the initial assessment (prior to any or just as initial intervention takes place), then will continue 30minutely for 90minutes whilst in the ED. If patient is admitted to the ward then hourly-4hrly depending on the patients clinical condition or wards protocol.]
Secondary Outcome Measures
NameTimeMethod
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