Evaluation of treatment of chronic constipation using combination of Rosa damascene and brown sugar in comparison with polyethylene glycol in children over 12 months old

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20090908002434N8

Enrollment

100

Registered

2020-11-15

Start date

2020-10-05

Completion date

Unknown

Last updated

2020-11-30

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: "intervention group" rosemary extract and red sugar based on the matching of the desired active ingredient in which 1cc / kg / day of rose syrup and rose with 1cc / kg / day of polyet

Eligibility

Sex/Gender

All

Age

12 Months to 18 Years

Inclusion criteria

Inclusion criteria: Children over 12 months of age with Functional Constipation no underlying disease such as Hirschsprung's disease and metabolic and hypothyroidism

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Defecation less than or equal to two times a week. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.;Fecal incontinence equal or more than once a week. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.;History of stool retention. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.;History of hard or painful defecation. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.;Large fecal mass in the rectum. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.;History of thick stools that may block the toilet. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.;Appetite disorder. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.;Bad Breath. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.;Abdominal pain. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.	—

Measure

Time frame

Defecation less than or equal to two times a week. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.;Fecal incontinence equal or more than once a week. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.;History of stool retention. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.;History of hard or painful defecation. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.;Large fecal mass in the rectum. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.;History of thick stools that may block the toilet. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.;Appetite disorder. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.;Bad Breath. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.;Abdominal pain. Timepoint: Start treatment, two weeks later and four weeks later. Method of measurement: Questionnaire.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbbas Avaz Pour

Shiraz University of Medical Sciences

abbas.avazpour@yahoo.com+98 71 3647 4298

Outcome results

None listed

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