The effect of administration time of oral iron preparations on hemoglobin response
- Conditions
- Iron deficiency anemia.Iron deficiency anemia
- Registration Number
- IRCT20210503051166N2
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 196
Patients with iron deficiency anemia based on iron profile study such as serum iron, ferritin, and transferrin saturation percent
Hemoglobin level less than 11 mg/dl
Not suffering from chronic liver disease (normal bilirubin, LFT<2 times normal), or other chronic inflammatory diseases based on initial evaluation
Not suffering from active malignancy based on initial evaluation
Not suffering from active infection based on initial evaluation
Not suffering from any of the malabsorption syndromes based on the initial evaluation
Patients with cardiovascular risk factors
Suffering from any chronic kidney disease, liver disease, all types of cancer, infections and autoimmune diseases
The patient's lack of consent to participate in the plan
Having dyspepsia and intolerance to iron food products
High CRP levels at study entry
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Increase in hemoglobin level. Timepoint: before intervention and 4 weeks after intervention. Method of measurement: Hemoglobin concentration in complete blood count test.
- Secondary Outcome Measures
Name Time Method