CTRI/2022/08/044745尚未招募2 期
Comparative clinical study on the efficacy of Devadarvadi kashaya tablet and Ashotone tablet in Sutika wellbeing.
Parul Institute of Ayurved0 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
- 2 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
- •Primi or Multipara (upto G2) with full term normal delivery (Beyond 37 weeks of
- •gestational), who are willing to take part in the study and ready to sign informed
- •written consent form.
- •Women who delivered with or without Episiotomy.
- •Even preterm delivery beyond 32 weeks, subjects with anemia >7gms %, history of Sickle Cell anemia, instrumental/ Vacuum deliveries will be incorporated.
排除标准
- •1. Women who delivered with the lower segment caesarian section.
- •2. Parturient with history of eclampsia or PPH.
- •3. Patient with history of hyper/hypotension, hyper/hypoglycemia or any other chronic systemic disease.
- •4. Women with Thyroid dysfunction during pregnancy or gestational diabetes mellitus or IUD or Still birth or APH.
- •5. Severe anemia (ââ?°Â¤7 gm/dl).
研究者
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