MedPath

Effect of vitamin D on intensity of dysmenorrhea

Phase 3
Conditions
Primary dysmenorrhea.
Primary dysmenorrhea
N94.4
Registration Number
IRCT20180218038789N3
Lead Sponsor
Qazvin University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
92
Inclusion Criteria

Moderate to severe primary dysmenorrhea (score above 4 based on visual pain scale)
Being Single
Being at reproductive ages (18 to 35 years)
Student of Qazvin University of Medical Sciences
Willingness to participate in the study

Exclusion Criteria

Presence of secondary dysmenorrhea and its underlying factors such as history of endometriosis, adenomyosis, subacute endometritis, pelvic inflammatory disease, copper intrauterine devices, ovarian cysts, congenital pelvic malformations and cervical stenosis based on individual statement
Concurrent use of corticosteroids, anticonvulsants, anti-TB, anti-hypertension, which interfere with the absorption of vitamin D.
Use vitamin D or calcium supplements
Probability of graduation during the follow-up period
History of known mental illness based on individual statement
Drug addiction based on self disclosure

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Intensity of dysmenorrhea pain. Timepoint: Before, Immediately, 1, 3, 6 months after intervention. Method of measurement: Visual analogue scale.
Secondary Outcome Measures
NameTimeMethod
Duration of dysmenorrhea pain. Timepoint: Before, immediately, 1, 3 and 6 months after the intervention. Method of measurement: Individual report of pain duration by day.;Need to use pain killer. Timepoint: Before, immediately, 1, 3 and 6 months after the intervention. Method of measurement: Individual report of need to use pain killer.;Menstrual distress. Timepoint: Before, immediately, 1, 3 and 6 months after the intervention. Method of measurement: Moos questionnaire of menstrual distress.
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