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

Not Applicable

Recruiting

• Conditions: Primary dysmenorrhea.; Pain and other conditions associated with female genital organs and menstrual cycle

• Registration Number: IRCT20180221038821N4
• Lead Sponsor: Gonabad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 30 November 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 60

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

Reluctance to continue participating in the study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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.