CTRI/2022/08/044856
尚未招募
2 期
A randomized control trial to determine the efficacy and schedule of oral calcium supplementation for prevention of adverse citrate reaction in plateletpheresis donors.
AIIMS Delhi0 个研究点目标入组 0 人待定
概览
- 阶段
- 2 期
- 干预措施
- 未指定
- 疾病 / 适应症
- 未指定
- 发起方
- AIIMS Delhi
- 状态
- 尚未招募
- 最后更新
- 3年前
概览
简要总结
暂无简介。
研究者
入排标准
入选标准
- •Donors eligible for plateletphersis as per the Drugs and Cosmetics Act 1940; Rule 1945 (Amendment 2020\) (DCA)
排除标准
- •i.Donors eligible as per the DCA but found to be reactive in transfusion transmitted infectious disease screening testing
- •ii.Donors already on calcium, or Vitamin D supplements.
- •iii.Donors with incomplete procedure due to reason other than hypocalcemic adverse reactions.
- •iv.Donors with incomplete procedure due to technical reasons.
结局指标
主要结局
未指定
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