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Comparison of the effect of Sorbitol and Polyethylene Glycol on Constipation in Children with chronic functional constipation

Comparison of the effect of Sorbitol and Polyethylene Glycol on constipation in children with chronic functional constipation

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240507061697N1
Enrollment
126
Registered
2025-01-14
Start date
2024-12-20
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Chronic Functional Constipation. Constipation

Interventions

Intervention 1: Intervention group: Children with chronic functional constipation whom received polyethylene glycol powder from Sepidaj Pharmaceutical Company, marketed under the brand name Pedrolax w

Sponsors

Ilam University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 10 Years

Inclusion criteria

Inclusion criteria: Children with chronic functional constipation taking Polyethylene Glycol Children with Chronic Functional Constipation taking Sorbitol

Exclusion criteria

Exclusion criteria: Children who received treatment for constipation in the two weeks prior to study enrollment Children with intellectual disabilities or metabolic disorders, such as hypothyroidism Children diagnosed with irritable bowel syndrome (IBS) according to Rome III Criteria Children with Hirschsprung disease, spinal abnormalities, or anorectal pathologies

Design outcomes

Primary

MeasureTime frame
Frequency of abdominal pain. Timepoint: Frequency of abdominal pain before intervention and 2 weeks after intervention. Method of measurement: Physical Examination.;Stool consistency. Timepoint: Stool consistency before intervention and 2 weeks after intervention. Method of measurement: Bristol Stool Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactErfan Abbasi

Ilam University of Medical Sciences

erfan.erfan.7500@gmail.com+98 84 3372 5058

Outcome results

None listed

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