MedPath

A study of Gunja taila on Migraine.

Phase 1/2
Not yet recruiting
Conditions
Migraine, unspecified. Ayurveda Condition: ARDHAVABHEDAKA,
Registration Number
CTRI/2023/06/054160
Lead Sponsor
Gurukul Campus Uttrakhand Ayurved University Haridwar
Brief Summary

*Ardhavabhedaka* is a type of *Shiro-rog*, characterised by severe tearing and pricking pain in *Manya, Bhru, Shankha, Karna, Akshi* and *Lalata* which is paroxysmal in nature and is very much resembles to Migraine. In *Bhaisajyaratnavali, Acharya Govinddas Sen* has indicated *Gunja Taila nasya* in A*rdhavabhedaka*. In this study we will administered *Gunja Taila* as *Nasya* in Group A and Placebo (Roasted wheat powder capsules) in Group B.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria
  • 1.Age group 16-60 years.
  • 2.Patient will be selected irrespective of sex,religion,occupation,habitat etc.
  • 3.Patient with any classical symptoms of Ardhavabhedak/Migraine.
  • 4.Patient having recurrent attack of headache with or without nausea,vomiting,aura.
  • 5.Patient fit for Nasya karma.
Exclusion Criteria
  • 1.Patient unfit for Nasya karma as mentioned in Ayurvedic reference books.
  • 2.Patient having history of Head Trauma.
  • 3.Pregnant women and Lactating mothers.
  • 4.Patient having symptoms of Ophthalmoplegic migraine and Retinal migraine.
  • 5.Known cause of headache like epilepsy, cysticercosis, brain tumor.
  • 6.Systemic disorders that may interfere in the line of treatment like heart disease, kidney disease, hyperthyroidism, hypothyroidism.
  • 7.Secondary headache caused by meningitis, tumor, encephalitis, cervical spondylitis, refractive errors and infectious disease.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improvement will be assessed on the basis ofOutcome will be assessed at baseline, 33 day, 48 day and 63 day
subjective parameters- by Grading scale adopted for this study and MIDAS SCALE.Outcome will be assessed at baseline, 33 day, 48 day and 63 day
Secondary Outcome Measures
NameTimeMethod
T.L.CD.L.C

Trial Locations

Locations (1)

Gurukul Campus Uttarakhand Ayurveda University Haridwar

🇮🇳

Hardwar, UTTARANCHAL, India

Gurukul Campus Uttarakhand Ayurveda University Haridwar
🇮🇳Hardwar, UTTARANCHAL, India
Dr Swati Bhatt
Principal investigator
9761008941
dr.swatibhatt2405@gmail.com

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.