Evaluation effect of Curcumin in patients with Primary Dysmenorrhea

Phase 3

Recruiting

• Conditions: Primary dysmenorrhea.; Primary dysmenorrhea; N94.4

• Registration Number: IRCT20180404039187N8
• Lead Sponsor: Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 9 November 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 80

Inclusion Criteria

Patients with Primary Dysmenorrhea
Aged 18 to 35 years old
Having at least four recent consecutive painful menstrual cycles during the past six months
Bleeding of 3 to 7 days during the menstruation

Exclusion Criteria

Taking contraceptives within the past two months
Using intra-uterine device or drugs containing Curcumin within the past six months
Smoking an alcohol consumption
Malignancy

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Severity of pain during menstruation. Timepoint: before intervention and 1, 2 months after intervention. Method of measurement: visual analogue scale.;Needs of NSAIDs. Timepoint: before intervention and 1, 2 months after intervention. Method of measurement: DN4 Questionnaire.