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The Effect of Myrtus Communis L. fruit syrup in women bleeding

Assessment the Effect of Myrtus Communis L. (Myrtle) fruit syrup (B 438 syrup) in hypermenorrhea

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201109077511N1
Enrollment
30
Registered
2012-03-21
Start date
2012-05-21
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

hypermenorrhea. Excessive and frequent menstruation with regular cycle

Interventions

Intervention 1: Syrup (drug), 3 times daily for a week starting menstruation, 1 tablespoon each half hour after meal. The trend for 3 menstrual cycles (every month for 7 days) is repeated. Interventio
Treatment - Drugs
Placebo
Syrup (placebo), 3 times daily for a week starting menstruation, 1 tablespoon each half hour after meal. The trend for 3 menstrual cycles (every month for 7 days) is repeated.
Syrup (drug), 3 times daily for a week starting menstruation, 1 tablespoon each half hour after meal. The trend for 3 menstrual cycles (every month for 7 days) is repeated.

Sponsors

Medical faulty, Shahed University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patient satisfaction; outpatients aged 20- 55 years with excessive uterine bleeding that have a negative pregnancy test and they are not lactating; Endometrial thickness in ultrasound is normal; Gynecologic examination is normal; The Pap smear is normal; concurrent hormonal therapy, herbal and other medicinal plants are not used; there are no chronic disease like diabetes, lupus and thyroid problems; there is no organic disease such as uterus or ovaries or other malignancies; Intramural fibroids larger than 5 cm sub mucosal or not; Bleeding is more than 7 days and or Course is less than 21 days. Exclusion criteria: use of hormonal drugs in the study; Use of mefenamic acid in the study; Patients who are experiencing possible side effects; Patients who require surgical intervention and have the other; Patients with a personal request to withdraw from the study; bleeding during the study is so severe that emergency action is required.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Menstrual period duration. Timepoint: at the end of each cycle. Method of measurement: Questionnaire.;Intensity of menstrual bleeding. Timepoint: at the end of each cycle. Method of measurement: Questionnaire.;Hemoglobin. Timepoint: before & after the study. Method of measurement: cell counter.

Secondary

MeasureTime frame
Drug side effect. Timepoint: at the end of study. Method of measurement: questionniare.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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