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Instrument Development For Ayurvedic Fume Nasal Inhalation (Dhooma Nasya)

Designing and developing a portable device for Dhooma nasya. - PDND

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/066600
Enrollment
48
Registered
2024-05-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Parul Institute of Ayurved
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Subject which are fit for Dhooma nasya Karma. 2.Subject are Irrespective of Gender, Religion and Disease. 3.Subject Age between 18-60yrs.

Exclusion criteria

Exclusion criteria: 1.Subject which are unfit for Dhooma nasya Karma. 2.Subject Age less then 18yrs and more then 60yrs are excluded.

Design outcomes

Primary

MeasureTime frame
Designing and Developing a portable device for Dhooma NasyaTimepoint: Eight months—

Secondary

MeasureTime frame
Observe the effect of Dhooma nasya karma with use of classical method and technically modified Dhooma nasya deviceTimepoint: Group A- Dhooma nasya administeration for 7 days with classical method Group B- Dhooma nasya administeration for 7 days with device—

Countries

India

Contacts

Public ContactDr Sangeeta H Toshikhane

Parul Institute of Ayurved

sangeeta.toshikhane26791@paruluniversity.ac.in9964596479

Outcome results

None listed

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