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The effects of olive leaf extracts on hemorrhoid disease symptoms

The effects of olive leaf extracts on hemorrhoid disease symptoms

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220724055547N1
Enrollment
180
Registered
2022-11-14
Start date
2022-10-23
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Hemorrhoid. Hemorrhoids and perianal venous thrombosis

Interventions

Intervention 1: Intervention group 1: Treated with a combined ointment containing Aburihan anti-hemorrhoid ointment and 1% olive leaf extract (Dana Kasian Company)for 21 days, 3 times a day or as dire

Sponsors

Khoram-Abad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Grade 1 to 3 hemorrhoid disease Not taking medicine for hemorrhoid disease in the last 14 days Non-pregnant women Having a moderate to severe pain score age between 18 to 65

Exclusion criteria

Exclusion criteria: History of allergy or anaphylaxis to the drugs used Lack of consent to participate in the study Suffering from other colon diseases

Design outcomes

Primary

MeasureTime frame
Pain due to hemorrhoid disease after using the ointment. Timepoint: Days 0, 3, 7, 14, 21 after the start of the intervention. Method of measurement: Assignment of a score between 1 to 10 by the patient.;Itching due to hemorrhoid disease after using the ointment. Timepoint: Days 0, 3, 7, 14, 21 after the start of the intervention. Method of measurement: Assignment of a score between 1 to 4 by the patient.;Bleeding due to hemorrhoid disease after using the ointment. Timepoint: Days 0, 3, 7, 14, 21 after the start of the intervention. Method of measurement: Assignment of a score between 1 to 4 by the patient.;Other side effects after using the ointment. Timepoint: Days 0, 3, 7, 14, 21 after the start of the intervention. Method of measurement: Assignment of a score between 1 to 4 by the patient.;Patients satisfaction after using the ointment. Timepoint: 21 days after the start of the intervention. Method of measurement: very much, much, medium, weak based on the patient's estimation and feeling of satisfaction.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGolsa Farzan

Khoram-Abad University of Medical Sciences

golsa.f.96@gmail.com+98 66 3322 8981

Outcome results

None listed

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