Primary care Respiratory Upper respiratory tract infection
Conditions
Interventions
300 children will be randomised to receive either normal saline nose spray or sodium cromoglycate 4% nose spray every 2 h (during waking hours) for the first 2 days, and every 4 h for a further 5 days
Sponsors
Medical Research Council (MRC) (UK)
Eligibility
Inclusion criteria
Inclusion criteria: Children aged from 6 months to 6 years with suspected acute viral URTI for less than 36 h
Exclusion criteria
Exclusion criteria: Children with: a history of having taken cromolyns or steroids within the previous week; carers who are incapable of giving informed consent or unable to keep symptom diaries; an established complication requiring immediate hospitalisation, or for whom the clinician plans to prescribe antibiotics at the first consultation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| CARIFS Scale Score | — |
Secondary
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Countries
United Kingdom
Outcome results
None listed