a study to evaluate the effectiveness of a protocol in allergic rhinitis (vathika prathisyaya)

â??â??A pre and post clinical study to evaluate the effectiveness of toxicological treatment protocol in allergic rhinitis (vathika prathisyaya)â??â??

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2017/09/009916

Enrollment

100

Registered

2017-09-26

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: null- allergic rhinitis mild-moderate

Interventions

Intervention1: 1.vishavilwady gulika 2.surasadi gana kashyayam 3.amritha ghrithm 4.lakshdadi dhoopana churnam: vishavilwady gulika 2no.s and surasadi gana kashayam 45ml,twice daily for 2 weeks. amrith

Eligibility

Inclusion criteria

Inclusion criteria: those patients who had recurrence after standard allopathic and ayurvedic care,with history of exposure to allergens,total IgE levels higher than 100IU/ml

Exclusion criteria

Exclusion criteria: ASTHMA DNS ENT Disorders food allergy persistent severe allergic rhinitis patients with less age than 20yrs and higher than 40 yrs of age pregnant ladies and lactating mothers patients who failed to give consent and failed to follow up

Design outcomes

Primary

Measure	Time frame
total 5 symptom scoring-nasal congestion,rhinorrhea,sneezing,occular pruritis,nasal pruritis symptoms of prathisysya -dryness throat,palate, and lips,headache,nasal congestion,rhinorrhea graded based on severityTimepoint: 2 weeks,4 weeks,6 months and 12 months	—

Secondary

Measure	Time frame
nilTimepoint: nil	—

Countries

India

Contacts

Public ContactPREETHI MOHAN

AMRITA VISWAVIDYA PEETHAM

drpreeti94@gmail.com9447320363

Outcome results

None listed

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