Skip to content

Comparing the Effects of Vasadi Kwath and Amrutadi Kwath in Gout Treatment

A RANDOMIZED CLINICAL STUDY TO COMPARE THE EFFICACY OF VASADI KWATH AND AMRUTADI KWATH IN THE MANAGEMENT OF VATARAKTA W.S.R. TO GOUT - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080722
Enrollment
60
Registered
2025-02-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: M109- Gout, unspecified

Interventions

None listed

Sponsors

Dr. VJD Gramin Ayurved Mahavidyala
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients showing classical signs and symptoms of Vatarakta as described in Ayurvedic Samhita. 2.Unilateral first MTP joint attack. 3.Sr Uric acid level ranges between 7 to 12 mg/dl 4.Patients between the age of 20 to 60 years. 5.Patients from all socio-economic status. 6.Either gender.

Exclusion criteria

Exclusion criteria: 1.Patients not willing. 2.Patients with peptic ulcer. 3.Pregnant and lactating women. 4.Patients who have not been affected by NSAIDs. 5.Patients who have past history of malignant tumour. 6.Sr. Uric acid level below 7 mg/dl and above 12 mg/dl. 7.Patients with Sr. Creatinine level more than 2 mg/dl. 8.Patients below 20 years of age and above 60 yers of age. 9.Patients having any major chronic or acute systemic or surgical pathology.

Design outcomes

Primary

MeasureTime frame
1)Shool (Joints of hands and feet, Parva sandhi, etc.) 2)Stambha (Stiffness) 3)Daha (Burning Sensation) 4)Kandu (Itching) 5)Shoth (Swelling) 6)Twakkrushnata (Discoloration) Timepoint: 15Days, 30 Days, 45 Days after starting treatment

Secondary

MeasureTime frame
Decrease symptoms completelyTimepoint: 18 Months

Countries

India

Contacts

Public ContactDrJayashree Katole

DR VJD Gramin Ayurved Mahavidyalaya,Patur

drjrkatole@gmail.com9423847608

Outcome results

None listed

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