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临床试验/CTRI/2023/08/055952
CTRI/2023/08/055952尚未招募2 期

CLINICAL STUDY OF TILADI KWATHA ORALLY AND SHATPUSHPA SIDDHA TAILA NASYA IN THE MANAGEMENT OF PUSHPAGHNI ? (PCOS) - CSTKST

Post Graduate Institute of Ayurved, Jodhpur Rajasthan0 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
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

  • 1.Patients diagnosed cases of PCOS by the Rotterdam criteria.
  • 2.Age: Patients aged between 16-40 years.
  • 3. The patients who are fit for the Nasya procedure were only considered for the study.
  • 4. Patients willing for Informed consent.

排除标准

  • Patients having any other disease causing oligomenorrhea and anovulation excluding PCOD on the above criteria.
  • Patients using oral contraceptive pills.
  • Pregnant and lactating women.
  • Patients suffering from thyroid abnormalities, Hyperprolactinemia, adrenal hyperplasia etc.
  • Patients with any organic reproductive system abnormalities like hydrosalpinx, endometriosis, fibroid uterus, carcinoma of reproductive organ and sexually transmitted disease (STDs), Human Immunodeficiency Virus (HIV), Hepatitis B Surface Antigen (HBsAg).
  • Systemic disorders like-uncontrolled diabetes mellitus, chronic liver disease, renal disorder, Uncontrolled hypertension, Diagnosed case of any type of malignancy.
  • Patients who are contraindicated for Nasya like, Nasal polyp etc.

研究者

发起方
Post Graduate Institute of Ayurved, Jodhpur Rajasthan

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