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The effectiveness of a topical form of Cassia fistula L. on Constipatio

Phase 3
Conditions
Functional Constipation.
Constipation
Registration Number
IRCT20170929036482N2
Lead Sponsor
Traditional Medicine school of Tehran University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
150
Inclusion Criteria

Age between 18 to 50 years
Confirmation of functional constipation diagnosis based on Rome III criteria

Exclusion Criteria

Pregnancy, , , , , , , ,
Lactating women
History of abdominal surgery
Gastrointestinal bleeding
Psychosis
Recent surgery
Serious Heart or Liver diseases or Endocrine disorders (Diabetes, Thyroid dysfunction)
Cancer
Anemia

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Frequency of defecation per week. Timepoint: Before the study, end of week 2, end of week 4. Method of measurement: A questionnaire based on Rome III criteria.;Frequency of hard stool. Timepoint: Before the study, end of week 2, end of week 4. Method of measurement: A questionnaire based on Rome III criteria.;Frequency of straining during defecation. Timepoint: Before the study, end of week 2, end of week 4. Method of measurement: A questionnaire based on Rome III criteria.;Frequency of sensation of incomplate evacuation. Timepoint: Before the study, end of week 2, end of week 4. Method of measurement: A questionnaire based on Rome III criteria.;Frequency of sensation of anorectal blockage. Timepoint: Before the study, end of week 2, end of week 4. Method of measurement: A questionnaire based on Rome III criteria.;Frequency of manual maneuvers to facilitate defecation. Timepoint: Before the study, end of week 2, end of week 4. Method of measurement: A questionnaire based on Rome III criteria.
Secondary Outcome Measures
NameTimeMethod
Skin complication at the site of topical use. Timepoint: Before study, end of week 2, end of week 4. Method of measurement: A questionnaire.;Any possible complications. Timepoint: Before study, end of week 2, end of week 4. Method of measurement: A questionnaire.
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