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临床试验/CTRI/2025/09/095246
CTRI/2025/09/095246尚未招募2/3 期

A Comparative Clinical Study To Asses The Efficacy Of Shirashooladi Vajra Rasa Along With Devdarvyadi Roll On And Shirashooladi Vajra Rasa In Vattaj Shirashool WSR To Tension Headache

Dr DY Patil school of Ayurveda Deemed to be University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年10月16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
60
试验地点
1
主要终点
Improvement of clinical symptoms-pain at temporal region ,pain in center of forehead,pain aggravated at night time ,stiffness in neck region ,phtophobia,giddiness

研究概览

简要总结

TITTLE -A COMPARATIVE CLINICAL STUDY TO ASSES THE EFFICACY OF SHIRASHOOLADI VAJRA RASA ANLONG WITH DEVDARVYADI ROLL ON AND SHIRASHOOLADI VAJRA RASA IN VATTAJ SHIRASHOOL WSR TO TENSION HEADACHE

The effectiveness of shirashooladi vajra rasa alone vs the combination of Devdarvyadi roll on and Shirashooladi vajra rasa in Vattaj Shirashool with tension headache can be studied .Snehan is main chikitasa in vataja shirashool so devdarvyadi roll on contains all the drugs that pacify the vatta dosha and to make it more fesiable we will convert  it into roll on .Total 30 patients will be added in both groups group A will receive Devdarvyadi roll on and shirashooladi vajra rasa Group B will receive only shirashooladi vajra rasa .During first day of assesment patients will be selected on the basis of symptoms of vattaj shirashool pain at forehead pain in temporal region pain at night etc; range of neck motion criteria will also be noted and headache impact test score will be filled on 1st and last day to asses the progress. Outcomes will be assess on improvement in range of neck motion and reduction in symptoms of vattaj shirashool and improvement in Headache impact test

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

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

入选标准

  • Patient of either sex or aged between 18 to 60yrs 2)Patient willing and able to participate in study 3)Patients presenting with symptoms of tension headache and vataj shirashool as described in subjective criteria.

排除标准

  • Age group less than 18 years and more than 60 years 2)Patient is not willing to participate in study 3)Patients with underlying pathological conditions like trauma Meningities Brain tumors Migraine headache through refractive errors will be excluded 4)Patient with history of addictive drugs drinks smokers alcohol consumers 5)Pregnant and lactating women 6)Through subjective criteria scoring 4&5 very severe and most severe pain will be excluded.

结局指标

主要结局

Improvement of clinical symptoms-pain at temporal region ,pain in center of forehead,pain aggravated at night time ,stiffness in neck region ,phtophobia,giddiness

时间窗: 28days

2)Improvement in Headache impact score 6 test filled n 1st and last day of follow up

时间窗: 28days

3)Improvement in range of neck motion criteria

时间窗: 28days

次要结局

  • Recurrence of clinical symptoms of vattaj shirashool -pain in temporal region,pain in centre of forehead,pain aggravated at night time,stiffness in neck region photophobia,giddiness(28 days)

研究者

发起方
Dr DY Patil school of Ayurveda Deemed to be University
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

DR PRAJAKTA SHRINIVAS PARUNDEKAR

Dr DY Patil School of AyurvedaDeemed To Be University ,Nerul ,Navi Mumbai 400706

研究点 (1)

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