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Effect of flixweed in children constipation

Effect of Sisymbrium Sophia on functional constipation in comparison with poly ethylene glycol in 2-12 y/o children

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013011412126N1
Enrollment
120
Registered
2013-01-21
Start date
2013-01-15
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

functional constipation. constipation

Interventions

Intervention 1: control: polyethylene glycol 3gr before 4y/o and 6 gr 5 y/o and upper for 3 weeks and daily(Qod). Intervention 2: case: descurainia sophia syrup 2gr before 4y/o and 3gr 5y/o and upper
Treatment - Drugs
control: polyethylene glycol 3gr before 4y/o and 6 gr 5 y/o and upper for 3 weeks and daily(Qod)
case: descurainia sophia syrup 2gr before 4y/o and 3gr 5y/o and upper for 3 weeks and daily(Qod)

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 12 Years

Inclusion criteria

Inclusion criteria: Iclusion criteria: functional constipation based on Rom3 criteria and age between 2 to 12 years. Exclusion criteria: organic cause constipation and irritable bowel syndrome criteria based on Rome3.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Frequency of bowel habit per week. Timepoint: before intervention, 0-1-2-3 week after intervention. Method of measurement: rome 3 standard questionnaire.;Frequency of bulky solid stool per week. Timepoint: before intervention, 0-1-2-3 week after intervention. Method of measurement: standard q rome3.;Frequency of encopresis per week. Timepoint: before intervention, 0-1-2-3 week after intervention. Method of measurement: standard q rome3.;Frequency of painful bowel habit per week. Timepoint: before intervention, 0-1-2-3 week after intervention. Method of measurement: standard q rome3.;Frequncy of bloody stool per week. Timepoint: before intervention, 0-1-2-3 week after intervention. Method of measurement: standard q rome3.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMajid Nimrouzi

Tehran university of medical sciences

nimruzim@sums.ac.ir+98 71 1233 7589

Outcome results

None listed

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