CTRI/2024/08/072349尚未招募2 期
A comparative clinical study to evaluate the efficacy of Krishna Tila Kashaya and Kulatthadi Kashaya in the management of Artavakshaya - NI
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
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.Patients aged between 18-35 years.
- •2.Both married and unmarried women.
- •3.Bleeding, spotting less than 2 days.
- •4.Pad used 1 per day.
- •5.Infrequent menses at intervals longer than 35 days.
- •6.Patients presenting with the Pratyatma Lakshana of Artava Kshaya. (Uchitakala Adarshana, Alpata, Yonivedana)
排除标准
- •1.Patient with a systemic disorder like DM, HTN, TB, Asthma, Congenital abnormalities.
- •2.Patient with mal-nutrition, severe anaemia (Hb less than 8gm percent) pregnant and Lactating women, women using OCP and IUCD, congenital anomalies of uterus or ovaries
研究者
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