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The effect of probiotic use in children with functional constipation

The effect of probiotic use in children with functional constipation

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210525051398N1
Enrollment
150
Registered
2021-05-30
Start date
2021-05-31
Completion date
Unknown
Last updated
2021-06-21

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

Conditions

Functional Constipation. Constipation

Interventions

Intervention 1: Intervention group: The first group is dissolved Kidi Lactate probiotic powder in a dose of 1 sachet per day in water and 1 g / kg body weight of water-soluble polyethylene glycol powd

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 15 Years

Inclusion criteria

Inclusion criteria: Children with functional constipation Between 2 to 15 years old

Exclusion criteria

Exclusion criteria: Diseases of the large and small intestine Sensitivity to polyethylene glycol Intestinal obstruction Kidney or heart failure

Design outcomes

Primary

MeasureTime frame
Number of bowel movements during one week. Timepoint: Number of bowel movements during one week at the beginning of the study (before the intervention) and 7 and 14 days after taking probiotics. Method of measurement: The required information is collected by asking the parents and recorded in the prepared questionnaire.;Number of unwanted bowel movements during the day. Timepoint: Number of unwanted bowel movements during the day at the beginning of the study (before the intervention) and 7 and 14 days after taking probiotics. Method of measurement: The required information is collected by asking the parents and recorded in the prepared questionnaire.;Number of painful bowel movements in a week. Timepoint: Number of painful bowel movements during one week at the beginning of the study (before the intervention) and 7 and 14 days after the start of probiotic use. Method of measurement: The required information is collected by asking the parents and recorded in the prepared questionnaire.;The number of times abdominal pain occurs in a week. Timepoint: The frequency of abdominal pain during one week at the beginning of the study (before the intervention) and 7 and 14 days after taking probiotics. Method of measurement: The required information is collected by asking the parents and recorded in the prepared questionnaire.;Determination and comparison of fecal consistency. Timepoint: Determination and comparison of fecal consistency at the beginning of the study (before the intervention) and 7 and 14 days after probiotic use. Method of measurement: The required information is collected by asking the parents and recorded in the prepared questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPegah Kaveh

Islamic Azad University

pgh.kaveh@gmail.com+98 31 3433 1295

Outcome results

None listed

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