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Effect of Ficus carica and Juglans regia product on the treatment of functional Constipation of older Adults

Evaluation of the effect of Ficus carica and Juglans regia product on the treatment of functional Constipation of older Adults: A double blind randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200714048108N1
Enrollment
90
Registered
2020-09-19
Start date
2020-09-05
Completion date
Unknown
Last updated
2020-10-06

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: For each patient is given 15 cc of fig and walnut syrup one hour before bedtime for two consecutive weeks. Intervention 2: Control group: For the control group, e

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
55 Years to 85 Years

Inclusion criteria

Inclusion criteria: Forcing in more than more than 3 times a week Hard or bullet-like stools in more than 3 times a week Feeling of incomplete emptying in more than 3 times a week Feeling of anorectal obstruction or cramping in more than 3 times a week Need for manual maneuvers to facilitate defecation in more than 3 times a week Spontaneous bowel movements less than 3 times a week

Exclusion criteria

Exclusion criteria: Dissatisfaction to participate in the research Intolerance to taking drugs Possible side effects (in the form of nausea, vomiting, severe abdominal pain, allergic reactions, etc.) Improper use of medication

Design outcomes

Primary

MeasureTime frame
Gastrointestinal pain. Timepoint: Painless stools was measured at the beginning of the study (before the intervention), after the last treatment session, and 30 days (one month) after the last treatment session. Method of measurement: General Mizaj questionnaire.;Constipation. Timepoint: Assessing constipation was measured at the beginning of the study (before the intervention), after the last treatment session, and 30 days (one month) after the last treatment session. Method of measurement: General Mizaj questionnaire.;Stool type. Timepoint: Stools with less stiffness intervention), after the last treatment session, and 30 days (one month) after the last treatment session. Method of measurement: General Mizaj questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaeed Jodi Khajeh

Tabriz University of Medical Sciences

saeedjodi1348@gmail.com+98 914 308 1743

Outcome results

None listed

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