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Comparison of oral consumption of pomegranate peel and Mefenamic Acid on Efrat tams disease

Comparison of oral consumption extract hydrophilia of pomegranate peel and Mefenamic Acid on menorrahagia disease

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017090936103N1
Enrollment
60
Registered
2017-11-18
Start date
2017-11-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Menorrhagia. excessive and frequent menstruation with regular cycle

Interventions

Intervention 1: Intervention 1. A 250 mg capsule extract of pomegranate peel is consumed after each meal in 7 days of menstruation for three cycles. Intervention 2: Intervention 1. A 250 mg capsule of
Treatment - Drugs
Intervention 1. A 250 mg capsule extract of pomegranate peel is consumed after each meal in 7 days of menstruation for three cycles.
Intervention 1. A 250 mg capsule of Mefenamic Acid is consumed after each meal in 7 days of menstruation for three cycles.

Sponsors

Shahed University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients with high or long uterine bleeding who have had a negative pregnancy test; and are not breast-feeding; in ultrasonography their thickness of endometrium is normal; there is no mass of adnexa and ovaries except for a simple cyst less than two centimeters; genecology examination and Pap smear tests are normal; they’re not taking other hormonal and anticoagulant drugs like aspirin; or herbal drugs and teas; they do not have systemic or organic diseases and bleeding disorders; In the ultrasound the size of the uterus is less than 10 cm; there is no submucosal or intramural fibroma; and sub-serous fibroma is not bigger than 4 cm; they do not use IUD; and do not have BMI greater than 30; CBC and Hb are not less than 10. Exclusion criteria: Taking hormonal drugs during the study; experiencing possible side effects like anemia (Hb less than 10); needing surgery or other interventions; leaving the study on personal requests; requiring emergency procedures during the study due to severe bleeding; occurrence of pregnancy; and experiencing serious side effects due to the drugs.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bleeding Volume. Timepoint: One month before, first, second and third month after intervention. Method of measurement: Pictorial Blood Loss Assessment Chart.;Bleeding Volume. Timepoint: One month before, first, second and third month after intervention. Method of measurement: Pictorial Blood Loss Assessment Chart.

Secondary

MeasureTime frame
Hb level. Timepoint: Before and 3 months after intervention. Method of measurement: Lab test.;Quality of life. Timepoint: Before and 3 months after intervention. Method of measurement: Menorrhagia questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGholamreza Salsali

Shahed University

gh.salsali@shahed.ac.ir+98 21 5121 3565

Outcome results

None listed

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