CTRI/2018/03/012845招募中未知
Safety and efficacy of oral iron syrup in adolescents, pregnancy and postpartum.
试验速览
- 阶段
- 未知
- 状态
- 招募中
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
入选标准
- •1. Female subjects
- •2. Age between 12-40 years
- •3. Willingness and ability to participate in study procedures
- •4. Hb of 11 g/dL or less
- •5. For postpartum women, 10 days or less postpartum
- •6.For pregnant women, Gestational age beyond 12 weeks
- •7. Willingness to provide the writeen informed consent
排除标准
- •1. History of anemia other than iron deficiency anemia
- •2. Recent blood transfusion
- •3. Current treatment with myelo suppressive therapy or asthma therapy
- •4. Intolerance to iron derivatives
- •5. For postpartum women, the following exclusion criteria will also apply:
- •1.Significant vaginal bleeding
- •2. History of blood loss due to delivery being considered for blood transfusion
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