A study to compare efficacy of AGNIMANTH MOOL CHOORNA AND HARIDRAKHANDA CHOORNA in management of SHEETPITTA.(URTICARIA)

â??A RANDOMISED CONTROLLED CLINICAL STUDY OF AGNIMANTH MOOL CHOORNA AND HARIDRAKHANDA CHOORNA IN THE MANAGEMENT OF SHEETPITTA.

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/06/043083

Enrollment

Registered

2022-06-08

Start date

Unknown

Completion date

Unknown

Last updated

2022-06-27

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

Conditions

Health Condition 1: L00-L99- Diseases of the skin and subcutaneous tissue

Interventions

Intervention1: Agnimanthmool choorna: Agnimanthmool choorna Is Prepared As Per Ayurved Text.Dose-3 gms,Frequency-twice a day,Duration-1 month,Route- oral Control Intervention1: Haridrakhanda Choorna:

Eligibility

Inclusion criteria

Inclusion criteria: Patients between ages 20-60 yrs irrespective of gender,religion & occupation. Patients having Granthokt lakshanas of sheetpitta

Exclusion criteria

Exclusion criteria: Patients having any associated major illness like 1) Renal failure. 2) Diabetes mellitus. 3) Systemic Lupus Erythematous. 4) Rheumatic disorders. 5) Any type of malignant diseases e.g. Leukaemia metastatic cancer etc. Patient taking treatment from any other pathy for the same problem. Hypersensitivity reactions to any drug.

Design outcomes

Primary

Measure	Time frame
To compare the efficacy of AGNIMANTH MOOL CHOORNA AND HARIDRAKHANDA CHOORNA in the management of Sheetpitta(Urticaria).Timepoint: 30 Days on follow up on 7 days.	—

Secondary

Measure	Time frame
To Study The Side Effects of Drug If Any.Timepoint: 30 Days	—

Countries

India

Contacts

Public ContactDR YOGENDRA YASHWANT MORE

PDEAs College of Ayurveda And Research Centre Akurdi Pune

khobragaderupali19@gmail.com

Outcome results

None listed

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