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Comparison of therapeotic effect of probiotic with PEG in children functional constipation.

Comparison of therapeotic effect of probiotic with PEG in children functional constipation.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013112415511N1
Enrollment
120
Registered
2013-12-13
Start date
2013-08-21
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

Constipation. Constipation

Interventions

Intervention 1: Group 1: Polyethylene glycol (PEG) + placebo (n = 40). Intervention 2: Group 2: Probiotic + placebo (n = 40). Intervention 3: Group 3: polyethylene glycol (PEG) + probiotic (40).
Placebo
Treatment - Drugs
Group 1: Polyethylene glycol (PEG) + placebo (n = 40)
Group 2: Probiotic + placebo (n = 40)
Group 3: polyethylene glycol (PEG) + probiotic (40)

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 16 Years

Inclusion criteria

Inclusion criteria: nclusion criteria: children 2-16 years of age with chronic functional constipation associated with any disease.Exclusion criteria: Children diagnosed with IBS criteria ROME III;Treatment of constipation in the two weeks prior to study entry; Children with mental retardation or metabolic diseases (eg, hypothyroidism); Children with Hirschsprung's disease or anorectal anomalies injury or pathology; Children with a history of stomach or intestinal surgery; Children under medical treatment affecting the GI such as cisapride; Motilium, erythromycin and loperamide

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Defecation frequency per week. Timepoint: Baseline and then. Method of measurement: Questionnaire.;Stool consistency. Timepoint: Baseline and then. Method of measurement: Questionnaire.;Read Ndad having abdominal pain and painful defecation. Timepoint: Baseline and then. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Headache. Timepoint: Baseline and then. Method of measurement: Checklist.;Nausea and vomiting. Timepoint: Baseline and then. Method of measurement: Checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarjan Habibi

Arak University of Medical Sciences

mary_jane612000@yahoo.com+86 33134716

Outcome results

None listed

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