IRCT20210730052015N1招募中3 期
Comparison of the effectiveness of treatment of iron deficiency anemia with daily vs. every other day oral iron supplementation
适应症
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 376
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 15 years 至 50 years(—)
- 性别
- Female
入选标准
- •Age = 15 years and less than 50 years
- •outpatients Women with iron deficiency with ferritin less than 30 micrograms per liter
- •No pregnancy
- •No breastfeeding right now
- •Absence of comorbidities (ckd, DM, IHD, etc.)
- •Lack of known history of inflammatory bowel disease
- •Lack of known history of celiac disease
- •No known history or thalassemia
- •No known hereditary bleeding disorder
- •Do not take multivitamin and mineral supplements (35 mg or more of essential iron per day) in the 2 weeks prior to randomization.
- •No allergy to oral iron
- •Lack of intravenous iron therapy in the last 12 weeks
- •Do not receive anticoagulants (eg warfarin, apixaban, debigatran, adoxaban, Riveroxban)
- •Lack of creatinine clearance less than 30 ml per minute
- •Lack of hemoglobin less than 80 g / l with active bleeding
- •No chemotherapy planned for the next 12 weeks.
- •No surgery is scheduled for the next 12 weeks.
排除标准
- •Intolerance or non-response to oral iron gluconate, sulfate or fumarate in the last 12 weeks
- •Received frequent anemia treatments and are resistant to anemia treatment.
- •Dissatisfaction to participate in the study or lack of cooperation and consent to continue treatment
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