CTRI/2017/05/008524招募中2 期
A Controlled Comparative clinical Study of Efficacy of Bala Taila in the Management of Episiotomy Wound
Parul Institute of Ayurved0 个研究点目标入组 40 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- 入组人数
- 40
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 Primipara patients who undergo vaginal delivery with episiotomy will be selected.
- •2 Patient between ages 20 to 35 will be selected.
- •3 No history of disease impaired wound healing.
- •4 Those patient who ready to sign the inform consent form will be included only.
排除标准
- •1 Multipara.
- •2 Patients with 3rd and 4th degree perineal tear or injury to rectum / urethra
- •3 Patients with any other major illnesses e.g. HIV, HbSAg, VDRL positive,cancer.
- •4 Patients with history of delayed wound healing, IDDM, gestational diabetes, congenital bleeding disorders.
研究者
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