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The effect of curcumin on painful symptoms of endometriosis

Phase 3
Recruiting
Conditions
Endometriosis.
Endometriosis
Registration Number
IRCT20120718010324N66
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
68
Inclusion Criteria

Women with endometriosis whose endometriosis has been confirmed by laparoscopy
Women with symptomatic endometriosis
Not taking of anti-inflammatory or hormonal medication in the last three months
Not having endometrial hypoplasia or neoplasia
Women who are married and sexually active

Exclusion Criteria

Women who have allergic to ginger plants
Women with gallstones, jaundice due to bile duct obstruction, and acute biliary colic
Women with gastrointestinal diseases

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Painful symptoms of endometriosis. Timepoint: Before the intervention and 8 weeks after starting of intervention. Method of measurement: ENDOPAIN-4D questionnaire.
Secondary Outcome Measures
NameTimeMethod
Quality of life. Timepoint: Before the intervention and 8 weeks after starting the intervention. Method of measurement: EHP-30 questionnaire.;Severity of dysmenorrhea. Timepoint: The first three days of the menstrual cycle before the intervention and then the first three days of the next two cycles. Method of measurement: VAS ruler.;Frequency of analgesic use. Timepoint: During the intervention. Method of measurement: Checklist.;Side effects. Timepoint: During the intervention. Method of measurement: Side effects checklist.
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