Dysmenorrhea and premenstrual symptoms. Primary dysmenorrhea
Conditions
Interventions
Intervention 1: Intervention group: For the intervention group, black cohosh herbal medicine with the medicinal name of Simi Fogel, which Gol Daru Company manufactures, will be used. This medicine is
Sponsors
Khoy University of medical science
Eligibility
Sex/Gender
Female
Age
18 Years to 30 Years
Inclusion criteria
Inclusion criteria: Regular menstruation 21-35 days Age 18-30 years insensitivity to black cohosh and other herbal medicines containing phytoestrogens (soybeans, flax seeds, lentils, mung beans, etc.) According to the person's statement Not taking any medication to treat dysmenorrhea at the same time as research Having primary dysmenorrhea (with VAS score = 4) Not having liver problems according to the person's own statement not married Complaining of menstrual symptoms (cramps, headache, abdominal pain, mood disorders, etc.)
Exclusion criteria
Exclusion criteria: First semester students Use of other herbal medicines and painkillers. The occurrence of a stressful event (such as the death of a first-degree family member and the diagnosis of an incurable or incurable disease for a family member during the last three months) Abuse of tobacco and alcohol Having any acute or chronic disease (such as epilepsy, cardiovascular, digestive, liver, blood, endocrine) History of any female disease such as abnormal pelvic anatomy, lack of ovulation, or abnormal pattern of uterine bleeding Surgery in the last three months Insensitivity to black cohosh and other herbal medicines containing phytoestrogens (soybeans, flax seeds, lentils, mung beans, etc.)according to the person's statement. Taking antidepressants (such as serotonin and noradrenaline reuptake inhibitors, antihistamines, barbiturates, narcotics, diazepam, amphetamines, and cocaine)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Menstrual symptoms. Timepoint: The beginning of the study and the end of the study. Method of measurement: Menstrual symptoms intensity scale SSS.;Primary dysmenorrhea. Timepoint: The beginning of the study and the end of the study. Method of measurement: visual pain scale (VAS). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactnasrin zamiri-miandoab
khoy university of medical science
Outcome results
None listed