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A comparative evaluation of nasal (Nasya Karma) and oral administration of Brahmi Ghrita in healthy volunteers to evaluate the Memory boosting effect.

A comparative clinico-experimental evaluation of nasal (Nasya Karma) and oral administration of Brahmi Ghrita

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/08/006086
Enrollment
100
Registered
2015-08-11
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: Brahmi Ghrita Shamana Snehapana: Dose 16 ml Early in the morning (Rasayana kala),three sitting of 7 days, interval of 7 days (total-35 days) Anupana- Lukewarm water (Ushnodaka) Interven

Sponsors

Institute for post graduate teaching and research in Ayurveda Gujarat Ayurved University Jamnagar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Healthy Volunteers between age group of 20 years to 60 years

Exclusion criteria

Exclusion criteria: 1)Healthy Volunteer having age less than 20 years & above 60 years. 2)Classical Nasya Karma Ayogya and Abhyantar Snehapana Ayogya volunteers. 3) Diabetes, any cardiovascular diseases, renal diseases or any other disease effecting multiple body systems and pregnant women etc.

Design outcomes

Primary

MeasureTime frame
memory enhancer and cognitive enhancer in healthy volunteersTimepoint: 35 days

Secondary

MeasureTime frame
Analysis of effects of Brahmi Ghrita when administrated nasally (Nasya) and orally with same doseTimepoint: 35 Days

Countries

India

Contacts

Public ContactChetan M Gulhane

IPGT and RA GAU jamnagar

anup_thakar@yahoo.com9427776660

Outcome results

None listed

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