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A Study comparing two methods of Nasya in healthy individuals.

Crossover Comparative Clinical Study to Evaluate the Effect of Anu Taila Pratimarsha Nasya administered by Oil Based Capsules and Classical Method in Healthy Individuals - nil

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104130
Enrollment
100
Registered
2026-02-17
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Dr. Krishna S. Tailor
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Healthy individuals between the age of 18 60 years who are Yogya for Nasya. Subjects of either gender of all socioeconomic group. Subjects who are willing to give written consent.

Exclusion criteria

Exclusion criteria: Subjects below 18 years of age and above the age of 60 years. Subjects suffering from any systemic illnesses Subjects who are Ayogya for Nasya

Design outcomes

Primary

MeasureTime frame
Regarding subject preference based on their compliance by feedback formTimepoint: 8th day, 15th day

Secondary

MeasureTime frame
Standardization parameters confirming batch consistency. Absence of adverse events in participants post administration Stability data over a defined storage period (3-6months) under controlled conditions, including microbial and physical stability. Participant recorded scores on ease of use and convenience via feedback form. Requirement of assistance for administration. Physician reported preferences regarding safety, ease of administration, procedural hygiene and patient acceptability.Timepoint: 8th day, 15th day

Countries

India

Contacts

Public ContactDr Krishna S Tailor

Parul Institute of Ayurved and Research

dr.divyadeva3@gmail.com09844810958

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026