CTRI/2021/04/033099已完成3 期
A Prospective, Randomized, Open Label Study to Evaluate the Safety and Efficacy Of Mulmina Orange Amla Ready To Drink As A Supplement In Pregnant Woman at High Risk for Preeclampsia
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 60
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 volunteer aged more than 18 to 45 years
- •2.If pregnant, should have completed 1st trimester of the pregnancy
- •3.Pregnant Woman At High Risk For Preeclamsia
- •4.Willing to give written consent to participate
排除标准
- •1.Patients with preexisting severe systemic disease necessitating long term medication.
- •2.Patients with known history of diabetes mellitus.
- •3.Evidence of significant uncontrolled co morbid disease which in the investigators opinion would jeopardize patient participation.
- •4.History of cancer including solid tumors hematologic malignancies and carcinoma in situ
- •5.Any neurological congenital or acquired vascular or systemic disorder which could affect any of the efficacy assessments.
- •6.Participation in the current or previous treatment with any approved or investigational health supplements during the past one month.
研究者
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