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An interventional trial to evaluate the effect of an Ayurveda treatment protocol in Allergic rhinitis

A pre and post-trial to evaluate the effect of an Ayurveda treatment protocol in Allergic rhinitis - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/085568
Enrollment
41
Registered
2025-04-24
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: J350- Chronic tonsillitis and adenoiditis

Interventions

None listed

Sponsors

DrPreethi Mohan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Those had recurrence of allergic rhinitis History of exposure to allergens Active age group of 20-40 years prone to exposure Clinical symptoms of mild allergic rhinitis and prathisyaya like rhinorrhoea, obstructed nose and sneezing. Positive skin prick test for aeroallergens Mild to moderate allergic rhinitis

Exclusion criteria

Exclusion criteria: Asthma DNS ENT disorders Food allergy Persistent severe allergic rhinitis Patients less than 20yrs and above 40 yrs Pregnant ladies & lactating mothers Patients who failed to give consent and who failed to follow up

Design outcomes

Primary

MeasureTime frame
SUBJECTIVE PARAMETER 1.Total Nasal Symptom Scores (TNSS) Each symptom (sneezing, congestion, itching, and rhinorrhea) is graded from 0-3 by the participants during the screening and subsequent visits OBJECTIVE PARAMETER Total IgE assessment Timepoint: baseline,2weeks,6week—

Secondary

MeasureTime frame
nilTimepoint: nil—

Countries

India

Contacts

Public ContactDrpreethi Mohan

amrita school of ayurveda

rameshnv@ay.amrita.edu09447320363

Outcome results

None listed

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