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Evaluation of efficiency of brihat dashamool taila nasya in management of vataj shirashool

A randomized controlled clinical trial to evaluate the efficiency of brihat dashamool taila nasya in the management of vataj shirashool - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/077342
Enrollment
60
Registered
2024-11-25
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: G891- Acute pain, not elsewhere classified

Interventions

None listed

Sponsors

Pdeas college of ayurved and research center
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patient showing at least two or more classical sign and symptoms of vataj shirashool 2 patient of age between 20 to 60 years irrespective of gender religion economic status 3 patient arha for nasya

Exclusion criteria

Exclusion criteria: 1 patient suffering from migraine cluster headache secondary headache such as medication overuse sinus headache and headache due to cervical spondylosis 2 pregnant and lactating women 3 known case of head injury 4 known case of inflammatory disease of supraclavicular organ

Design outcomes

Primary

MeasureTime frame
To compare the efficacy between brihat dashamool taila marsha nasya and ksheerabala taila marsha nasya for 7 days in the management of vataj shirashoolTimepoint: 7 days

Secondary

MeasureTime frame
NATimepoint: NA

Countries

India

Contacts

Public ContactDr Neha Joshi

PDEAS college of ayurved and research center

Drmayurashinde@gmail.com7276866831

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026