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To Design, Develop, Validate an Efficient Nasal Instillation instrument and to evaluate its efficacy in administration of Nasya

To design, develop, validate an efficient nasal instillation instrument and to evaluate its efficacy in administration of nasya in comparison with conventional method - An open labelled randomised comparative clinical trial - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/059449
Enrollment
100
Registered
2023-11-02
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

None listed

Interventions

None listed

Sponsors

Institute of Teaching and Research in Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Apparently healthy volunteers between the age group of 20 years to 40 years will be selected

Exclusion criteria

Exclusion criteria: Apparently healthy volunteers having age less than 20 years and above 40 years Classical Nasya ayogya volunteers Diabetes, any cardiovascular diseases, renal diseases or any other disease affecting multiple body system and pregnant women.

Design outcomes

Primary

MeasureTime frame
PGI memory scaleTimepoint: Before the intervention 0th day and 36th day—

Secondary

MeasureTime frame
Samyak Nasya Lakshana, Ayoga Nasya Lakshana & Atiyoga Nasya LakshanaTimepoint: After 7 days nasya in each course—

Countries

India

Contacts

Public ContactDr. Indu S.

Institute of Teaching and Research in Ayurveda

anup_Thakar@yahoo.com9427776660

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 27, 2026