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Comparison of the efficacy of Rosa damascena extract and mefenamic acid on the severity of the primary dysmenorrhea pai

Phase 3
Conditions
primary dysmenorrhea.
Primary dysmenorrhea
Registration Number
IRCT201207267618N2
Lead Sponsor
Research deputy of Tabriz University of Medical Sience
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
92
Inclusion Criteria

women with abdominal pain compatible with dysmenorrhea; being single; signing the informed consent sheet.
Exclusion criteria: pain severity more than 8 or less than 5 according to visual analogue scale system; history of genitourinary disease or abdomino-pelvic surgery; stressful event(loss); lack of compliancy; history of hypersensitivity to mefenamic acid; using drugs that interact with mefenamic acid.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of dysmenorrhea pain. Timepoint: before the first intervention, after the first intervention, before the second intervention, after the second intervention. Method of measurement: visual analogue scale.
Secondary Outcome Measures
NameTimeMethod
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