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Developing and Testing an Innovative Automated Nasya Therapy Device

Development And Validation of Automated Nasya Instrument Prototype - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079711
Enrollment
30
Registered
2025-01-29
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: 8- Other Procedures

Interventions

None listed

Sponsors

All India Institute of Ayurveda, Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients attending the Panchakarma OPD and IPD OF All India Institute Of Ayurveda undergoing the Nasya Procedure.

Exclusion criteria

Exclusion criteria: Patient not fit for Nasya karma. Patient not willing to undergo Nasya with instrument.

Design outcomes

Primary

MeasureTime frame
Development of automated Nasya InstrumentTimepoint: 0th day, 7th day—

Secondary

MeasureTime frame
To check the Patient s & Administrator s compliance during Nasya procedure done with Instrument & with Current methods.Timepoint: 0th day to 7th day—

Countries

India

Contacts

Public ContactProf Dr Anadaraman PV

All India Institute of Ayurveda

dr.ananthramsharma@gmail.com9495130595

Outcome results

None listed

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