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The effect of vitamin D supplementation on premenstrual syndrome(PMS)

Not Applicable
Conditions
premenstrual syndrome.
Registration Number
IRCT20180525039822N1
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
44
Inclusion Criteria

Age of 25-18 years
BMI in normal range
single
Serum vitamin D level is 30- 10 ng / ml
Having a regular menstrual cycle with intervals of 35 to 21 days
Not doing regular exercise
Students do not start or finish their studies in the semester

Exclusion Criteria

Acute and chronic diseases such as: cardiovascular, kidney, liver, diabetes, hypothyroidism, hyperthyroidism and asthma
Iron deficiency anemia (Anemia)
Depression and anxiety
Consumption of combined pills containing estrogen and progesterone
Take supplemental vitamin D in the last 3 months

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Serum level of interleukin 10 based on ELISA method. Timepoint: At the beginning of the study and after 4 months of intervention. Method of measurement: Blood sampling and serum level determination using ELISA kit.;Serum level of interleukin 12 based on ELISA method. Timepoint: At the beginning of the study and after 4 months of intervention. Method of measurement: Blood sampling and serum level determination using ELISA kit.;Serum level of total antioxidant capacity based on ELISA method. Timepoint: At the beginning of the study and after 4 months of intervention. Method of measurement: Blood sampling and serum level determination using ELISA kit.;Score of physical symptoms and mood syndrome in premenstrual syndrome in the symptom registration questionnaire. Timepoint: At the beginning of the study and after 4 months of intervention. Method of measurement: Premenstrual Signs Indexing Questionnaire (DSM-IV).
Secondary Outcome Measures
NameTimeMethod
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