跳至主要内容
临床试验/CTRI/2023/07/055258
CTRI/2023/07/055258尚未招募Unknown

comparative efficacy of shatapushpa taila nasya & shatapushpa churna in artavakshaya

Dr Lalita Prajapat0 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
Unknown
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

  • Age group 18- 40 yrs.
  • Interval between two menstrual cycles is greater than 35 days. (for the last 6 months approximately)
  • The duration of menstrual flow is 2 days or less. .(for the last 6 months approximately)
  • The quantity of menses is less than 20 ml.
  • Poly Cystic Ovarian Disease (PCOD) with the symptom of oligomenorrhea and hypomenorrhea.

排除标准

  • Patients below the age of 18 years and above the age of 40 years.
  • Positive history of venereal diseases (HIV, HBsAg, Anti HCV, VDRL, HPV, Genital herpes, etc.)
  • Pregnant women, lactating mothers.
  • Poly Cystic Ovarian Disease (PCOD) with menorrhagia.
  • Patient having organic pathology of uterus & adnexa like cervical carcinoma or any malignant growth.
  • Patients will not give consent to participate in the study.
  • Patients using oral contraceptive pills.
  • Patients who cannot attend follow-up regularly. Who is participating in another study.
  • Women suffering from Nasal polyp, D.N.S.(Deviated nasal septum), Rhinitis. Nasal tumor, and history of nasal surgery previous.

研究者

发起方
Dr Lalita Prajapat

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