Association between iron supplementation and vitamin D or vitamin D alone on bone metabolism and inflammation in women.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion criteria: Healthy; Non-smoker; Non-pregnant; Non-lactating; Body mass index: 18.5-29.9 kg/m2; Ferritin less than 30 ng/ml; Hemoglobin less than 12 g/dl; 25 hydroxy vitamin D less than 30 ng/ml. Exclusion criteria: Amenorrhea; Menopause; Minor Thalasemia; Hemochromatosis; Inflammatory bowel diseases; Crohn's disease; Gastric ulcer; Celiac disease; Gastrointestinal bleeding diseases; Renal diseases; Blood donation during past 3 months; Iron or Vitamin D supplement use during past 3 months.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 25 hydroxy vitamin D. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample. | — |
Secondary
| Measure | Time frame |
|---|---|
| Hematocrit. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Mean Cell Vollum. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Hemoglobin. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Serum iron. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Ferritin. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Transferrin. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Transferrin saturation. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Total Iron Binding Capacity. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Alkaline phosphatase. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Parathyroid hormone. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;C-terminal telopetide x. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Osteocalcin. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Highly-sensitive C Reactive Protein. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Tumor Necrosis Factor Alpha. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Interleukin 6. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Total Antioxidant Capacity. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Malodialdehyde. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Lipid profile. Timepoint: At baseline and the end of the study. Method of measurement: Blood sample.;Fasting Blood Sugar. Timepoint: At baseline and the end of the study. Method of measurement: Blood sa | — |
Countries
Iran (Islamic Republic of)
Contacts
Nutrition and health group