CTRI/2020/02/023125尚未招募4 期
Efficacy, Safety and Acceptability of Intravenous Versus Oral Iron Therapy in Postpartum Anemia - A Randomised Controlled Trial
Department of Obstetrics And Gynecology0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
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
- •Patients with Hemoglobin between 8-10gm/dl, 36-48 hours after delivery.
- •Group A will be treated with Intravenous Iron .
- •Group B will be treated with Tablet Iron.
排除标准
- •Peripartum Blood Transfusion
- •Intolerance To Iron Derivatives
- •Clotting disorders
- •Patients with Anemia other than that caused by blood loss secondary to delivery and iron deficiency anemia.
研究者
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