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Comparison of the Effect of Herbal Tea with Achillea Millefolium Capsule on the severity of Primary Dysmenorrhea in Students Residing in Dormitories of Gonabad University of Medical Sciences

Comparison of the Effect of Herbal Tea with Achillea Millefolium Capsule on the severity of Primary Dysmenorrhea

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180221038821N4
Enrollment
60
Registered
2020-11-07
Start date
2020-11-21
Completion date
Unknown
Last updated
2020-11-30

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

Conditions

Primary dysmenorrhea. Pain and other conditions associated with female genital organs and menstrual cycle

Interventions

Intervention 1: Intervention group: Group receiving Yarrow extract capsule. Yarrow hydroalcoholic extract was obtained with the help of a biochemist and injected in special capsules in the amount of 1

Sponsors

Gonabad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Informed consent Being 15 to 45 years old Having regular menstruation with intervals of 21 to 35 days according to the statements of research units Having dysmenorrhea pain with a score higher than 5 according to the visual pain scale No history of physical illnesses such as asthma, allergies, migraines, diabetes, thalassemia, hypertension, thyroid, cardiovascular disease and no pelvic inflammatory disease diagnosed uterine problems such as abnormal bleeding and ovarian cysts based on patient statement Do not take hormonal drugs and oral contraceptives for the past three months No accidents during the last six months, according to research units Lack of sensitivity to medicinal and chemical plants according to the statements of research units The onset of menstrual cramps coincides with the onset of menstrual bleeding or a few hours before the onset of menstruation and lasts for a maximum of 48 to 72 hours, according to research units. No abnormal bleeding during the study Do not use housing while studying Absence of any effects indicating an allergic reaction based on the researcher's observation and the statements of research units Use yarrow capsule or tea according to the recommended method

Exclusion criteria

Exclusion criteria: Reluctance to continue participating in the study

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: At the beginning of the study (before the intervention) and at the end of the first, second and third days of each menstrual cycle. Method of measurement: Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactIman Ghorbany Moghaddam

Gonabad University of Medical Sciences

imanghorbany135213@gmail.com+98 51 5725 0773

Outcome results

None listed

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