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The effect of Cassia Fistula syrup in geriatrics consipation

The effect of Cassia Fistula syrup in geriatrics consipation in comparison with the lactulose

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200105046009N3
Enrollment
70
Registered
2020-07-17
Start date
2020-06-22
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

geriatrics consipation. Constipation

Interventions

Intervention 1: Intervention group: Cassia fistula syrup prepared and standardized in the Laboratory of Medicinal Plants of Babol School of Traditional Medicine, 30 cc daily (in three separate doses)

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 60 years Diagnosis of constipation based on ROME IV criteria

Exclusion criteria

Exclusion criteria: The presence of organic diseases is the basis for constipation Presence of cardiovascular disease, neurological disease, metabolic disease or mental disorders. Hematologic disease or malignant tumor (unless recurrent in the last 5 years) History of alcohol use or substance abuse

Design outcomes

Primary

MeasureTime frame
Frequency of defecation. Timepoint: Number per week. Method of measurement: counting and recording the number of defecation per week.

Secondary

MeasureTime frame
Feeling of incomplete emptying after defecation. Timepoint: Before intervention and 7 and 14 days after intervention. Method of measurement: Daily questionnaire on quality of defecation.;Number of times of manual maneuver in defecation. Timepoint: Before intervention and 7 and 14 days after intervention. Method of measurement: Daily questionnaire on quality of defecation.;Stiffness of stool. Timepoint: Before intervention and 7 and 14 days after intervention. Method of measurement: Visual Analogue Scale.;Quality of Life. Timepoint: Before intervention and 14 days after intervention. Method of measurement: Patient Assessment of Constipation Quality of Life Questionnaire (the Persian Version).

Countries

Iran (Islamic Republic of)

Contacts

Public Contactseyyed Ali Mozaffarpur

Babol University of Medical Sciences

seyyedali1357@gmail.com+98 11 3219 4730

Outcome results

None listed

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