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临床试验/CTRI/2020/04/024530
CTRI/2020/04/024530尚未招募2 期

A controlled comparative clinical study to evaluate Gandharyadi ghrita nasya and Go ghrita nasya in the management of Ardhavabhedaka w.s.r to Migraine.

未提供1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2020年1月5日最近更新:

试验速览

阶段
2 期
状态
尚未招募
入组人数
30
试验地点
1
主要终点
Response in headache

研究概览

简要总结

Migraine is a complex  neurological  disorder  that  manifests with  recurrent headache, nausea, vomiting, photophobia or phonophobia. Theprevalence of migraine  is 15% to 20%  in women  and 4% to 7%  in men. In children the prevalence may be as high as 17% and isequal in boys and girls. The highest prevalence  occur between the  ages of  25yrs and  55 yrs. Based  on  sign and  symptoms  of  Ardhavabhedaka. It can be compared  with migraine. Objective of this study is to compare theefficacy of Gandharyadi ghrita nasya and Go ghrita nasya along with internalmedication as Narikela khanda in the management of Ardhavabhedaka. Study will conduct in AIIA hospital with taken 15patients in each groups by block randomization. Diagnosis of patient will bedone according Intrernational headache society for migraine. Primary assessmentparameter will pain and secondary will quality of life. Total duration of thisstudy will be 53days.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
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 having symptoms of Ardhavabhedaka , 1) Ardha parshwa Shirashoola– unilateral headache 2) Bheda , Toda, Shoola- pulsating , throbbing type of pain 3) Pakshat, Dashahat ,Akasmat- paroxysmal episodes.
  • Prakasha Asahishnata- photophobia, Nausea (Hrillas), vomiting (Chardi).
  • phonophobia.

排除标准

  • Known cases of Secondary headache caused by sinusitis , meningitis , brain tumour, increased intra ocular pressure , malignant HTN.

结局指标

主要结局

Response in headache

时间窗: Assesment will be done on baseline, 23day, 38day and 53day.

次要结局

  • Overall improvement in quality of life.(assesment will be taken on baseline, on 23,38day and 53 day.)

研究者

发起方
未提供

研究点 (1)

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