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Zinc therapy in decreasing of dysmenorrhea.

Not Applicable
Conditions
dysmenorrhea.
primary dysmenorrhea
Registration Number
IRCT2012080610517N1
Lead Sponsor
Jahrom University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
120
Inclusion Criteria

history of regular menstrual cycles of 21-35 days with actual menstruation period of 3 to 7 days; if the participants experienced at least 4 consecutive painful menstruation periods in the past six months; the pain started one day before or at the starting day of menstruation and if dysmenorrhea disturbed daily activity of the patients for at least one day per month. After describing the study protocol, an informed consent was taken from the parents of patients. Enrolled patients underwent pelvic ultrasonography examination by a gynecologist. The patients were excluded if she had a clinically significant medical history or active disease; if a pelvic pathology was diagnosed by the gynecologist; if she used other medications or supplements and if she was not interested in using the drug and filling the pain charts of the study.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain duration. Timepoint: in 3 menstruation cyclein 3 month. Method of measurement: chart the day she has pain.;Pain severity. Timepoint: in 3 menstruation cyclein 3 month. Method of measurement: pain rating scale.
Secondary Outcome Measures
NameTimeMethod
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