Effect of probiotic supplements on children's asthma

Evaluation of the therapeutic effect of adding probiotic oral powder to standard treatment for the improvement of mild to moderate asthma in children

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180115038378N1

Enrollment

120

Registered

2018-09-12

Start date

2018-06-15

Completion date

Unknown

Last updated

2018-10-11

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

Conditions

Asthma. Asthma

Interventions

Intervention 1: Intervention group: Patients in this group consume 500 mg of Fmilact probiotics (produced by Zist Takhmir Company) for one month after three meals. Intervention 2: Control group: Patie

Eligibility

Sex/Gender

All

Age

3 Years to 8 Years

Inclusion criteria

Inclusion criteria: All 3 to 8 years old children with mild to moderate asthma

Exclusion criteria

Exclusion criteria: Age under 3 and over 8 People with seasonal allergies Children with severe and persistent asthma

Design outcomes

Primary

Measure	Time frame
Control of asthma symptoms. Timepoint: The 30th day after starting intervention. Method of measurement: PRAM standard questionnaire.	—

Secondary

Measure	Time frame
Disruption to go to the school due to a severe cough. Timepoint: The 30th day after starting intervention. Method of measurement: PRAM standard questionnaire.;The frequency of asthma attacks. Timepoint: The 30th day after starting intervention. Method of measurement: PRAM standard questionnaire.;Use Nasal spray or Nebulizer. Timepoint: The 30th day after starting intervention. Method of measurement: PRAM standard questionnaire.;The frequency of waking up at night. Timepoint: The 30th day after starting intervention. Method of measurement: PRAM standard questionnaire.;Control of cough symptoms. Timepoint: The 30th day after starting intervention. Method of measurement: PRAM standard questionnaire.	—

Measure

Time frame

Disruption to go to the school due to a severe cough. Timepoint: The 30th day after starting intervention. Method of measurement: PRAM standard questionnaire.;The frequency of asthma attacks. Timepoint: The 30th day after starting intervention. Method of measurement: PRAM standard questionnaire.;Use Nasal spray or Nebulizer. Timepoint: The 30th day after starting intervention. Method of measurement: PRAM standard questionnaire.;The frequency of waking up at night. Timepoint: The 30th day after starting intervention. Method of measurement: PRAM standard questionnaire.;Control of cough symptoms. Timepoint: The 30th day after starting intervention. Method of measurement: PRAM standard questionnaire.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Homan Tehrani

Sabzevar University of Medical Sciences

tehranih911@mums.ac.ir+98 51 4401 1604

Outcome results

None listed

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