ACTRN12616000470493
Completed
Not Applicable
A randomised controlled trial investigating Inhalation of heated, humidified air against placebo in people with the common cold: a feasibility study
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Common cold
- Sponsor
- Fisher & Paykel Healthcare
- Enrollment
- 30
- Status
- Completed
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Jackson score greater than or equal to 5
- •2\. Symptoms have been present for less than 48 hours at time of randomisation
Exclusion Criteria
- •1\. Age \<16 years or \>75 years
- •2\. Immunocompromised condition:
- •\- Conditions causing immunosuppression e.g. HIV/AIDS, active cancer
- •\- Currently prescribed steroids or other immunosuppressant medication
- •3\. A diagnosis of asthma, COPD or other significant respiratory conditions
- •4\. Nasal conditions such as deviated septum, chronic rhinitis, which, in the evaluation by the investigator, could impair nasal breathing.
- •5\. Use of cold remedies e.g. decongestants/cough linctus/sore throat lozenges within 6 hours of randomisation.
- •6\. Current use of antibiotics, steroids or inhaled medications.
- •7\. The investigator believes the participant or their care giver will be unable to safely use the myAIRVO 2 device following discharge
- •8\. Any other condition which, at the investigator’s discretion, is believed may present a safety risk or impact the feasibility of the study or the study results.
Outcomes
Primary Outcomes
Not specified
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