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A study to evaluate the efficacy of triphaladi taila nasya along with panchlavana ghritapana in the Management of vataja partishaya-allergic rhinitis

A clinical study to evaluate the efficay of triphaladi taila nasya along with panchlavana ghritpana in the management of vataja pratishyaya -allergic rhinitis - nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084070
Enrollment
30
Registered
2025-04-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: J069- Acute upper respiratory infection,unspecified

Interventions

None listed

Sponsors

Institute for ayurved studies and research Shri krishana AYUSH university
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: (1) Patients presenting with signs and symptoms of Vataja Pratishyaya mentioned in Ayurvedic Classics and Allergic Rhinitis according to Allopathic science (2) Patients willing to participate in the study (3) Patient of either sex (4) Patients between the age group of 16 60 yrs Exclusion Criteria (1) Patients having history of systemic disease as Diabetes Mellitus Hypertension Hypothyroidism (2) Patients suffering from gross deviation of nasal septum nasal tumours adenoid hyperplasia nasal polyps etc (3) Pregnant women (4) Patients not fit for Nasya therapy and Punchlavan ghritapana Discontinuation Criteria

Exclusion criteria

Exclusion criteria: (1) During the course of study if any serious condition or any serious adverse effects occur which require immediate and emergency treatment (2) Patient himself/herself wants to withdraw from the clinical study (3) If the patient fails to adhere to the protocol requirement

Design outcomes

Primary

MeasureTime frame
Reduction in sign and symptoms of Vataja Pratishyaya-Allergic Rhinitis. Timepoint: 35 Days

Secondary

MeasureTime frame
Improvement in quality of life of patient.Timepoint: 35 Days

Countries

India

Contacts

Public ContactDr Ashu

Institute for ayurved studies and research Shri krishana AYUSH university

drashukataria@gmail.com9416553131

Outcome results

None listed

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