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临床试验/CTRI/2022/10/046150
CTRI/2022/10/046150尚未招募1/2 期

Clinical study of narayana taila nasya in vataj artava dusti

Department of Panchakarma Gurukul campus UAU Haridwar1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2022年10月10日最近更新:
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试验速览

阶段
1/2 期
状态
尚未招募
发起方
入组人数
50
试验地点
1
主要终点
Improvement of assessment on basis of parameters like-
研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

Clinical study of Narayana Taila Nasya in Vataj Artava Dusti.

研究设计

研究类型
Interventional
盲法
Open Label

入排标准

年龄范围
15.00 Year(s) 至 40.00 Year(s)（—）
性别
Female

入选标准

  • •1.Patients with signs and symptoms of vataj artava dusti such as vikrit artava varna, ruja and artava which is ruksh, tanu, fenil, alpa, vichinna and vilambit.
  • •2.Patients with polycystic ovaries.
  • •3.Patients having altered FSH/LH.
  • •4.Patients with oligomenorrhoea, dysmenorrhoea, hypomenorrhea and amenorrhoea.

排除标准

  • •1.Patients with haemoglobin less than 7 g/dl.
  • •2.Patients with psychiatric disorders, epilepsy, heart disease, etc 3.Patients with known cases who are immunocompromised like HIV etc; who have haematological disorders such as haemophilia, leukemia etc.
  • •4.Patients with uncontrolled DM, HTN, Hypothyroidism.

结局指标

主要结局

Improvement of assessment on basis of parameters like-

时间窗: 1 day and 45 day

tanu, vilambit, vichinna artava.

时间窗: 1 day and 45 day

Artava varna (Colour), Artava pramana, Ruja (Pain), Rajaha sarava avidhi (Duration of menses), tanu, vilambit, vichinna artava.

时间窗: 1 day and 45 day

Fenil artava

时间窗: 1 day and 45 day

次要结局

  • •CBC(•Hb%)

研究者

发起方
Department of Panchakarma Gurukul campus UAU Haridwar
申办方类型
Government medical college

研究点 (1)

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