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?Studing the effect of Nano-curcumin and curcumoup in primary dysmenorrhea

Phase 3
Recruiting
Conditions
Dysenorrhea.
Primary dysmenorrhoea
Registration Number
IRCT20160813029327N11
Lead Sponsor
Islamic Azad University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
180
Inclusion Criteria

having primary dysmenorrhea
age of 18-27
Informed consent

Exclusion Criteria

pregnancy and lactation
hypersensitivity to the Curcumin products
using other drugs
asthma, GI tract diseases, cholelithiasis and obstruction of gull duct
intolerance of NSAIDs
using anti-coagulant agents
developing ovarian cysts
using OCPs

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Intensity of pain in primary dysmenorrhea. Timepoint: The measurement of intensity of pain, in first 3 days of 4 consecutive menstural period. Method of measurement: Visual Analogue Scale and quality of life questionnaire.
Secondary Outcome Measures
NameTimeMethod
Quantity of Mefenamic acid. Timepoint: Patients in first month will just use Mefenamic acid and in three following months will use mefenamic acid besides study drugs if it is necessary. Method of measurement: By questionnaire.
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