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Ayurvedic Management of Dushivishajanya SheetaPitta (Urticaria ) by Amrutarajanyadi Kashaya and Dushivishari Agada

Clinical efficacy of Amrutaranjanyadi Kashaya and Dushivishari Agada in the management of Dushivishajanya Sheetapitta w.s.r to Urticaria A Single Arm Open Labelled Clinical Trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084746
Enrollment
30
Registered
2025-04-15
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: L509- Urticaria, unspecified

Interventions

None listed

Sponsors

Institute of Teaching and Research in Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Age Group above 18 years and below 60 years 2 The patients having clinical signs & symptoms of Sheeta-pitta like, Raktavarna mandal Kandu, Toda, Vidaha (with or without Chardi, Jwara, Bhinna varna). 3 Chronicity more than 1 year 4 Ongoing modern treatment / Prolonged use of cosmetic items (upto 6 months) 5 Willing to accept the participation in the clinical trial.

Exclusion criteria

Exclusion criteria: 1 Chronicity less than year 2 Age below 18 years and above 60 years 3 Pregnant women and lactating mothers 4 Patients suffering from complicated systemic diseases like Diabetes mellitus, hypertension, Angio Oedema, kidney disease, Worm infestation and Liver disease will be excluded from the trial study. 5 Patients having history of taking drugs like - corticosteroids, anticonvulsant, NSAIDs 6 Patient who are not willing for inclusion in the study

Design outcomes

Primary

MeasureTime frame
Amrutarajanyadi Kashaya along with the Dushivishari Agada in the management of Dushivishajanaya SheetaPitta (Urticaria) like -Vartidanshta sansthana shotha, Raktavarna mandal, Kandu, Todadhikya, Vidhaha, Ksanikotpatti vinashaTimepoint: 6 WEEKS

Secondary

MeasureTime frame
Improvement in the quality of life of patients of urticaria.Timepoint: 6 WEEKS

Countries

India

Contacts

Public ContactDR MEGHA PANDYA

Institute of Teaching and Research in Ayurveda

drsud@itra.edu.in9687792882

Outcome results

None listed

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