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A Randomized Comparative Clinical Study Comparing Avapeedana Nasya with Shwasa Kuthara Rasa and Navana Nasya with Balahathadi Taila for the Treatment of Vataja Shirashoola Headaches

A randomised comparative clinical study to evaluate the efficacy of avapeedana nasya with shwasa kuthara Rasa and navana nasya with balahathadi taila in the management of vataja shiroshoola - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/07/113323
Enrollment
50
Registered
2026-07-03
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: G442- Tension-type headache

Interventions

None listed

Sponsors

Dr. Shreya Dipak Chougule
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients having classical symptoms of vataja shiroshoola Age group 20 year to 50 years Patients fit for nasya karma Patients willing for study trial with written informed consent Patients known history of hypertension Patients irrespective of gender religion socio economic status and locality

Exclusion criteria

Exclusion criteria: Pregnant women lactating mothers Patients suffering from any systemic disease such as diabetes mellitus II sinusitis Patients with having other neuralgic disorder such as trauma tumor malignancy

Design outcomes

Primary

MeasureTime frame
Reduction in the severity of Vataja Shirashoola assessed by the Vataja Shirashoola symptom scoreand improvement in pain intensity using the Visual Analogue Scale and HIT 6 questionary Assessments will be performed at baseline Day 0 after completion of treatment Day 7 and at follow-up Day 21 Timepoint: 21 days

Secondary

MeasureTime frame
NILTimepoint: Nil

Countries

India

Contacts

Public ContactDr I B Kotturshetti

Rajiv Gandhi education societys Ayurvedic medical College hospital and PG Research centre Ron

dr.basavarajvpp@gmail.com7337861654

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026