Clinical Trial of Amrutadi Syrup in Urticaria

An Open Labelled Randomized Controlled trial to evaluate the efficacy of â??Amrutadi Kashayaâ?? in the management of Sheetpitta with special reference to Urticaria - NIL

Status

Recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/12/078684

Enrollment

Registered

2024-12-27

Start date

Unknown

Completion date

Unknown

Last updated

2026-02-02

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

Eligibility

Inclusion criteria

Inclusion criteria: 1 The age limit is from 18 to 70 years.13 2 Patient suffering from Cardinals signs Mandalotpatti,Kandu and Associated symptoms of Sheetpitta (Urticaria) Daha,Toda,Jwar,Chhardi. 3 Patients with reocurrence within 6 months will be included. 4 Patients will be selected irrespective of Sex & Socioeconomic status.

Exclusion criteria

Exclusion criteria: 1 Pregnant and lactating women. 2 Patients with severe vomiting, diarrhoea and those who cannot take medicine orally. 3 Sheetpitta along with other chronic diseases and their associated complications. 4 Patient having major medical or surgical Illness. 5 Patients with a history of systemic illness like Diabetes mellitus, Hypertension, Endocrine disorder, Cardiac pathology, and Immunodeficiency disorders like AIDS. 6 Patient with drug-induced Sheetpitta (Urticaria).

Design outcomes

Primary

Measure	Time frame
To evaluate the efficacy of Amrutadi Kashaya in the management of SheetpittaTimepoint: 15 DAYS	—

Secondary

Measure	Time frame
NILTimepoint: NIL	—

Countries

India

Contacts

Public ContactDr Krutika Ramesh Jangale

MAMs Sumatibhai Shah Ayurved College Hadapsar Pune

krutikajangalekruz@gmail.com09168722181

Outcome results