Effect of capsule including Fenugreek seed versus placebo on severity and duration of pain in girls with primary dysmenorrhea
Phase 2
Recruiting
- Conditions
- Primary dysmenorrhoea.Primary dysmenorrhoea
- Registration Number
- IRCT201608019014N107
- Lead Sponsor
- Vice-chancellor for Research the Technology, Hamadan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
single; age of 19 to 35 years; moderate to severe primary dysmenorrhea; regular periods of 21 to 35 days.
Exclusion criteria: having chronic diseases; using any medications; sensitivity to Fenugreek; using any herbal drugs during the last 3 months; incomplete use of Fenugreek seed.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessing the severity of pain. Timepoint: every 8 hours during the period. Method of measurement: using McGill ruler pain.;Assessing the duration of pain. Timepoint: during the period. Method of measurement: on basis of day by taking history.
- Secondary Outcome Measures
Name Time Method othing. Timepoint: Nothing. Method of measurement: Nothing.