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Amirdha Gandhi Kukil Vallathy - Siddha management for Uthira Vaatha Suronitham (Rheumatoid Arthritis)

Preclinical and Clinical Validation of Herbo- Mineral Siddha Formulation Amirdha Gandhi Kukil Vallathy in Uthira Vaatha Suronitham (Rheumatoid Arthritis) pertaining to its Safety and Efficacy.

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/055008
Enrollment
40
Registered
2023-07-10
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Health Condition 1: M058- Other rheumatoid arthritis with rheumatoid factor

Interventions

Intervention1: Amirdha Gandhi Kukil Vallathy (AGKV).: Dose: 2 gm twice a day after food Vehicle : warm water Duration: 48 days Intervention2: Not applicable: It is a single arm study so Comparator

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: EULAR score >6 Patients willing to give informed consent Pt having score more than 6 are considered to have RA

Exclusion criteria

Exclusion criteria: Pregnancy and lactation Patients taking DMRAD s like Methotrexate Patients who had already participated in a new drug study in the past 3 months Known c/o Diabetes Mellitus Systemic Hypertension (SHT) Renal disease Cardiac disease Liver disorders Psoriatic arthritis

Design outcomes

Primary

MeasureTime frame
Response to treatment â?? Reduction in EULAR score from baseline to end of the studyTimepoint: Response to treatment â?? Reduction in EULAR score from baseline to end of the study

Secondary

MeasureTime frame
Reduction in clinical signs and symptoms by Decrease in Rheumatoid Arthritis Pain Scale (RAPS), Improvement in the quality of life by Modified health assessment questionnaire (MHAQ) will be assessedTimepoint: 48 days

Countries

India

Contacts

Public ContactDr CHRISTIAN L

CENTRAL COUNCIL FOR RESEARCH IN SIDDHA, MINISTRY OF AYUSH

drkkanakavalli@gmail.com9444122865

Outcome results

None listed

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