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Effect of homeopathy on the pain, menstrual symptoms and quality of life in patients with primary dysmenorrhoea

Not Applicable
Conditions
Primary dysmenorrhoea.
Primary dysmenorrhoea
Registration Number
IRCT201207063706N14
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
60
Inclusion Criteria

Eligibility criteria: age 18-27 years; single; having symptoms of primary dysmenorrhoea; pain severity of moderate to high (4.0-9.1); lack of pelvic and abdomen operations history; lack of allergy; non consumption of contraceptive drugs; non consumption of corticosteroids; non consumption of tobacco products; lack of allergy to Ibuprofen and the availability in visit specified days to visit.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of menstrual pain. Timepoint: During two months pre-intervention and two months after intervention. Method of measurement: Visual analogue scale (VAS).
Secondary Outcome Measures
NameTimeMethod
Menstrual symptom severity. Timepoint: During two months pre-intervention and two months after intervention. Method of measurement: Symptom severity scale (SSS).;Quality of life. Timepoint: at baseline and 2 months after starting intervention. Method of measurement: SF-36.
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