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Effect of beclomethasone in the control of pediatric asthma

The effect of inhaled beclomethasone with or without montelukast in the control of pediatric persistent asthma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017092036286N1
Enrollment
80
Registered
2017-10-17
Start date
2017-10-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Pediatric Persistent Asthma. Predominantly allergic asthma

Interventions

Intervention 1: First group: Patients of one group will receive 100 micrograms of inhaled beclomethasone three times a day with 5 mg of montelukast tablets daily. Intervention 2: Second group: Patient
Treatment - Drugs
First group: Patients of one group will receive 100 micrograms of inhaled beclomethasone three times a day with 5 mg of montelukast tablets daily.
Second group: Patients only will receive 100 micrograms of inhaled beclomethasone three times a day.

Sponsors

Vice- Chancellor for Research Technology Affairs, Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 10 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Pediatrics aged 6 to 10 years; Pediatrics with persistent asthma symptoms; referred to the Center during the study; Exclusion criteria: Pediatrics with lung infections; Pediatrics any underlying illness such as simultaneous cardiac disease; Antihistamine use; Having any illness; Taking other medications;

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

MeasureTime frame
Go to school. Timepoint: At the end of the treatment. Method of measurement: Take report from parent and completion in the questionnaire.;Night sleep quality (sleep deprivation). Timepoint: At the end of the treatment. Method of measurement: Take report from parent and completion in the questionnaire.

Primary

MeasureTime frame
FEV1. Timepoint: Before and 3 months after treatment. Method of measurement: With spirometry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Iraj Mohammadzadeh

Non-Communicable Pediatric Diseases Research Center, Health Research Institute, Babol University of

irjmoh2000@yahoo.com; faezeaghajanpour@yahoo.com;+98 11 3234 6963

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026