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Comparative efficacy of daily inhaled fluticasone propionate and episodic inhaled combined salmeterol/fluticasone propionate in children with recurrent wheezing

Comparative efficacy of daily inhaled fluticasone propionate and episodic inhaled combined salmeterol/fluticasone propionate in children with recurrent wheezing

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20180614002
Enrollment
Unknown
Registered
2018-06-14
Start date
2016-09-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

recurrent wheezing Efficacy&#44

Interventions

fluticasone propionate (IFP) MDI 125 mcg via cone spacer twice daily.,salmeterol/fluticasone propionate (ISFP) 25/125 mcg via cone spacer twice daily started at the onset of symptoms or signs of respi
6 puffs when having exacerbation.
Active Comparator Drug,Experimental Drug
Daily inhaled fluticasone propionate,episodic inhaled salmeterol/fluticasone propionate

Sponsors

Queen Sirikit National Institute of Child Health
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 15 Years

Inclusion criteria

Inclusion criteria: 1. History of recurrent wheezing at least 3 times/year and at least 2 of 5 symptom patterns tending to be asthma - Cough or wheeze more than 10 days during upper respiratory tract infection - Night worsening symptoms, cough or wheeze triggered by exercise and/or laughing and/or crying - History of atopy such as atopic dermatitis, allergic rhinitis - First degree relatives with asthma - Diagnosed asthma by spirometry

Exclusion criteria

Exclusion criteria: 1. Children who have history of using medications for controlling their recurrent wheezing symptoms such as Inhaled corticosteroids and/or leukotriene receptor antagonists before recruitment

Design outcomes

Primary

MeasureTime frame
Efficacy of symptom control 6 months Percentage and time to first exacerbation that needed systemic corticosteroids

Secondary

MeasureTime frame
Growth suppression and safety 6 months Increased height and adverse events

Countries

Thailand

Contacts

Public ContactJiratchaya Chamnanrua

Queen Sirikit National Institute of Child Health

jiratchaya0290@gmail.com0890543141

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026