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Traditional remedy of Foeniculum vulgare and Rosa Damascena on clinical symptoms of elderly patients with constipation

The Comparison of the effects of traditional remedy of Foeniculum vulgare and Rosa Damascena on clinical symptoms of elderly patients with functional constipation

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200108046056N1
Enrollment
60
Registered
2020-02-25
Start date
2020-02-20
Completion date
Unknown
Last updated
2020-03-24

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: Patients with chronic constipation treated with sachet of Roses Damascena and Foeniculum vulgare which was produced at the Kereman university of Medical Science, f

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: The elderly over 60 years of age mentally alert and able to answer questions constipation approved in accordance with Rome IV diagnostic criteria. informed consent. Having informed consent no history of gastrointestinal obstructive disorders. No history of gastrointestinal inflammatory diseases.

Exclusion criteria

Exclusion criteria: unwillingness to continue participation in the study at any time of the study. The occurrence of acute complications during the intervention. use of laxatives for constipation during the study. Reporting any signs suggesting an allergic reaction to Foeniculum vulgare and Rosa Damascena. Not taking regular medication

Design outcomes

Primary

MeasureTime frame
People with constipation who have 2 or more grade according to Rome 4 criteria. Timepoint: All of the above groups meet weekly on a weekly basis: initial visit and diagnosis before the intervention, one month after intervention and two month after the intervention intervention. Method of measurement: Questionnaire based on the international diagnostic criteria of chronic constipation-ROMIV.

Secondary

MeasureTime frame
Quality Of Life. Timepoint: Before the intervention. one month after intervantion, two month after the interventionintervention. Method of measurement: Patient Assessment of Constipation Quality of Life Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSedigh Khodabandeh Shahrki

Kerman University of Medical Sciences

S_khodabandeh@kmu.ac.ir+98 34 3132 5219

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 19, 2026