Comparative study of the effect of capsules Ginger-Lavender, Ginger with Mefenamic Acid on the severity of primary dysmenorrhea
- Conditions
- primary dysmenorrhea.Primary dysmenorrhoeaN94.4
- Registration Number
- IRCT20200525047565N2
- Lead Sponsor
- Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 90
1)Be 18 to 30 years old and single.
2)Experience menstrual pain in the first 3 days of bleeding for 3 consecutive periods in the last 6 months
3)People with primary dysmenorrhea whose pain intensity is moderate to severe according to McGill's pain ruler
4)Not known to be a person with a chronic illness (diabetes, high blood pressure, cardiovascular, infectious, liver, and epilepsy)
5)Do not have a specific gynecological disease that interferes with the study process
6)Have regular cycles with intervals of 21 to 38 days and the duration of menstruation is 3-7 days
7)Their body mass index is in the normal range of 19.8 to 26
8)According to the person, there are no symptoms such as burning, itching or abnormal discharge during the study.
9)Do not take any medications or supplements.
10)No herbal medicine has been used for 3 months before the intervention.01
11)Stressful factors such as parental separation, death of first-degree relatives, etc. should not be present in the last six months
1)Dissatisfaction or obedience of the person to continue participating in the study
2)Lack of proper use of medication or mefenamic acid
3)Take any herbal medicine while studying
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of primary dysmenorrhea. Timepoint: End of the third day of the cycle before the intervention, end of the third day of the first cycle and second cycle after the intervention. Method of measurement: Visual analog scale.
- Secondary Outcome Measures
Name Time Method Systematic symptoms. Timepoint: End of the third day of the cycle before the intervention, end of the third day of the first cycle and second cycle after the intervention. Method of measurement: Verbal rating scale.