Vataj Shiroroga Management With Snehan Nasya (Instillation of medicated oil in Nostrils)And Shirobasti Along With Oral Administration Of Pathyadi Kwath

Phase 2

Not yet recruiting

• Conditions: Acute pain, not elsewhere classified,

• Registration Number: CTRI/2020/09/027759
• Lead Sponsor: Govt Akhandanand Ayurved College

Brief Summary

To compare the efficacy of bala taila Shirobasti and bala taila Snaihik Nasya in the management of the Vataj Shiroroga is the main objective of the main objective of the Study.Patients will be Selected from Government Akhandanand Ayurved Hospital and Smt.Maniben Ayurved Hospital.They will be Treated with Bala Taila Shirobasti And Bala Taila Snehan Nasya Along With Pathyadi Kwath Orally.The Patients Will be assessed through VAS Criteria and other grading pattern.This Result will be analysed through Statistical Tests That will be required.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2020-08-09
• Study Start: 2020-09-17

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Clinically Diagnosed Patient of Vataj Shiroroga.

Exclusion Criteria

• Patients having age below 18Yrs and above 60 years Shirobasti Ayogya Nasya Ayogya Chronic sinusitis Referred headache from the ear, nose, eye and teeth.
• Secondary headache caused by meningitis, tumor, encephalitis, increase intra ocular Pressure, cervical spondylosis, hypoglycemia.
• Migraine Cerebral Haemorrhagic condition Brain injury Hydrocephalus Stroke Hypertension Pregnancy Neurological conditions: e.g. Trigeminalneuralgia Any other serious systemic illness.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Management of Vataj shiroroga relieves the Symptoms of Vataj Shiroroga	After the Completion of the treatment follow up of patient will be for 30 days with the interval of 15 days.

Secondary Outcome Measures

Name	Time	Method
Grading System of Vataj Shiroroga With VAS Criteria	After Completion of Treatment,Patient Will be Followed Up For 30 days

Trial Locations

Locations (1)

Government Akhandanand Ayurved hospital; 🇮🇳 Ahmadabad, GUJARAT, India

Government Akhandanand Ayurved hospital

🇮🇳Ahmadabad, GUJARAT, India

Kapadiya Umangkumar Jasvantbhai

Principal investigator

7990341453

kapadiyaumang16@gmail.com