Menometrorrhagia. Excessive and frequent menstruation with regular cycle
Conditions
Interventions
Intervention 1: Intervention group: Treated with 500mg capsules containing Capsella bursa-pastoris extract and starch, they will be placed three times a day between meals at 10am, 5am and will sleep f
Sponsors
Ghoum University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: Having a score more than 100 in Pictorial blood assessment chart Age between 18 to 50 years old The existence of uterine leiomyoma proven in ultrasound No use of any effective medication on menstrual bleeding such as: 0CP, ASA, anti-coagulant No regular use of special herbal remedy during the 2 weeks before the study No systemic disease such as :Thyroid, Hyperprolactinemia, Coagulopathy, hemoglobinopathy No abnormal pap smear No pregnancy No breast feeding
Exclusion criteria
Exclusion criteria: Incidence of surgical indications such as: abnormal bleeding disorder of vital signs, resistant anemia to usual treatments, severe anemia (hemoglobin below 7), acute pain, severe urinary symptoms or hydronephrosis The use of any hormone, anti-fibrinolytic or systemic glucocorticoid The use of Monoamine oxidase inhibitors allergy to the drug studied Pregnancy during the study Unwilling to continue participation in the study Incidence of side-effects requiring special treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Amount of Menstrual bleeding. Timepoint: One month before, first, second and third month after intervention. Method of measurement: Higam Chart.;Duration of Menstrual bleeding. Timepoint: One month before, first, second and third month after intervention. Method of measurement: Calendar.;Quality of life. Timepoint: Before and 3 months after intervention. Method of measurement: Menorrhagia questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Size of uterine leiomyoma. Timepoint: Before and 3 months after intervention. Method of measurement: Ultrasound.;Side effects of medication. Timepoint: 3 months after intervention. Method of measurement: Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAtiehsadat Danesh
Ghoum University of Medical Sciences
Outcome results
None listed