Vitamin D deficiency. Avitaminosis D
Conditions
Interventions
Intervention 1: Intervention group: This group will receive 2000 IU of oral vitamin D per day for 8 weeks. Intervention 2: Control group: The control group will receive placebo for 8 weeks.
Placebo
Control group: The control group will receive placebo for 8 weeks.
Sponsors
Vice chancellor for research of Shiraz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Inclusion criteria: At least 18 years of age; serum level of vitamin D 10- 30 ng/ ml; breast pain duration of =5 days per menstrual cycle; without any somatic or psychological disease. Exclusion criteria : Pregnant or lactating women; history of breast cancer; Stressful life events such as death of a family member.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in quality of life. Timepoint: Before and after intervention. Method of measurement: Quality of life questionnaire.;Change in lipid profile. Timepoint: Before and after intervention. Method of measurement: Lab test.;Change in C- Reactive protein. Timepoint: Before and after intervention. Method of measurement: Lab test. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFarideh Vaziri
Shiraz University of Medical Sciences
Outcome results
None listed