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临床试验/CTRI/2021/06/034009
CTRI/2021/06/034009尚未招募2/3 期

A RANDOMISED CONTROLLED CLINICAL TRIAL ON THE EFFICACY OF NIMBADI GUGGULU IN THE MANAGEMENT OF ARDHAVABHEDAKA(MIGRAINE)

DR AMRITHA MOHAN1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2021年6月20日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
40
试验地点
1
主要终点
Bheda Todavat Shula( Intensity of pain)

研究概览

简要总结

This is a randomised open label single centre trial comparing the efficacy of Nimbadi guggulu and Padhyadi ghanavati for 30 days in 40 patients with migraineheadache will be conducted in Alvas ayurveda medical college Vidyagiri Moodbidri Dakshina kannada INdia. Primaryoutcome measures will be relief from      Bheda Todavat Shula( Intensity of pain), Duration of single episode,  Frequency of  attack,Photophobia, nausea, vomiting in 90 days·

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研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Open Label

入排标准

年龄范围
16.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients aged 16 – 60 years irrespective of gender religion and socioeconomic status will be selected Patients presenting with clinical features of Ardhavabhedaka will be selected.

排除标准

  • Patients having other types of Shirashula apart from Ardhavabhedaka will be excluded.
  • Patients suffering from secondary headaches like sinusitis, meningitis etc.
  • will be excluded.
  • Patients with any other systemic diseases and pregnancy will be excluded.

结局指标

主要结局

Bheda Todavat Shula( Intensity of pain)

时间窗: 90 DAYS

Duration of single episode

时间窗: 90 DAYS

Frequency of attack

时间窗: 90 DAYS

Photophobia

时间窗: 90 DAYS

Nausea

时间窗: 90 DAYS

Vomiting

时间窗: 90 DAYS

次要结局

  • NOT APLICABLE(NOT APLICABLE)

研究者

发起方
DR AMRITHA MOHAN
申办方类型
Other [self]

研究点 (1)

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