Skip to content

Management of Tension headache by Shiroabhyanga and Pratimarsha Nasya with Tila Taila

Efficacy of Shiroabhyanga and Pratimarsha Nasya with Tila Taila in the management of Vataja Shirahshoola (Tension Headache)- A single Arm Clinical Trial - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084313
Enrollment
50
Registered
2025-04-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Institute of Teaching and Research in Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient aged between 18 to 60 years irrespective of the gender, cast, religion, occupation and financial status. 2.Patient willing to enrol for the study. 3.Patient having headache more than 3 months. 4.Patient having symptoms described in classical texts of Ayurveda and fulfilling ICHD-3 criteria 5. Shiroabhyanga and Pratimarsha Nasya Yogya as per classical texts.

Exclusion criteria

Exclusion criteria: 1. Patient having age below 18 years and above 60 years. 2. Patient is not willing to enrol for the study. 3. Patient having history of head injury 4. Secondary headache caused by migraine, ocular pathology, acute and chronic sinusitis, meningitis, encephalitis, cerebral abscess, intracranial tumour, cerebral haemorrhagic condition, lumbar puncture. 5. Known case of Hypertension and diabetes mellitus type 1 and type 2, having any major psychiatric illness 6. Pregnant women 7. Shiroabhyanga and Pratimarsha Nasya Ayogya as per classical texts.

Design outcomes

Primary

MeasureTime frame
1. Reduction in the symptoms of Vataja Shirahshoola(Tension headache). 2. Reduction in pain as measured by VAS score.Timepoint: 60 days

Secondary

MeasureTime frame
1. Reduction in the stress level as measured by Salivary cortisol, Galvenic skin resistance test and Hamilton anxiety rating scale. 2. Improvement in QOL.Timepoint: 60 days

Countries

India

Contacts

Public ContactVd Arpan A Bhatt

Institute of Teaching and Research in Ayurveda

vdarpansoniac@itra.edu.in9998968727

Outcome results

None listed

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