A clinical trial to study the effect of Agnikarma with Pathyadi kwatha & Viddha karma with Pathyadi kwatha in Ardhavabhedaka ( Migraine )_

Phase 2/3

Not yet recruiting

Conditions: Other specified disorders of nervous system in diseases classified elsewhere. Ayurveda Condition: ARDHAVABEDAKAH,

Registration Number: CTRI/2023/06/054109

Brief Summary: It is a randomized open label double arm controlledclinical study to compare the efficacy of Viddha karma during pain phase followed by which oraladministration of Pathyadi kwata 48ml in 2 divided dose for 2 weeks andAgnikarma during pain phase followed by withwhich oral administration of Pathyadikwata 48ml in 2 divided dose for 2 weeksArdhavabhedaka ( Migraine ) conducted in single center.

Detailed Description: Not available

Recruitment & Eligibility

Status: Not Yet Recruiting

Sex: All

Target Recruitment: 40

Inclusion Criteria

1.Patients between 20-45 years of age irrespective of sex, religion, occupation and socio -economic status and willing to participate and provide consent will be included 2.Patient having minimum of one episode of headache in 7 days 3.Patients with signs and symptoms of Ardhavabhedaka and migraine 4.Patients attending OPD during Vegavastha of Ardhavabhedaka (Pain Phase of Migraine).

Exclusion Criteria

1.Patients contraindicated for Agnikarma and Raktha mokshana as per classics.
2.Patients with other primary headache like tension, cluster headache 3.
Patients associated with secondary headache due to Glaucoma, Frontal sinusitis.
4.Patients with Systemic disorders ( Diabetes Mellitus, Hypertension).

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1.Improvement in the Subjective	one month
and objective parameters	one month
2.Improvementinthe HIT-6	one month
Questionnaire	one month
3.Sustained effect of treatment in	one month
reducingtheepisodesof	one month
Migraine	one month
4.Improvement changes in Midas	one month
5.A cost effective procedure which can be easily practiced	one month
during pain phase	one month

Secondary Outcome Measures

Name	Time	Method

Trial Locations

Locations (1): Sri Dharmasthala Manjunatheshwara institute of Ayurveda and hospital
🇮🇳
Bangalore, KARNATAKA, India
Sri Dharmasthala Manjunatheshwara institute of Ayurveda and hospital
🇮🇳Bangalore, KARNATAKA, India
DrPADMASHREE
Principal investigator
9986500898
padmashree@sdmayurbangalore.in