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临床试验/CTRI/2024/08/072349
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

Rajiv Gandhi University of health sciences0 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

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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