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Effect of Ayurveda Formulation in Hyperuricemia

Combined effect of Amritaguggulu and Amritashadangam Kashayam in the management of Hyperuricemia a pre test post test design - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/069098
Enrollment
31
Registered
2024-06-18
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: E790- Hyperuricemia without signs of inflammatory arthritis and tophaceous disease

Interventions

None listed

Sponsors

SILPA M R
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Participants without symptoms and with symptoms like pain and or tenderness of joint and serum uric acid level greater than 6.8mg/dL to 12mg/dl in males and greater than 5.7mg/dL to 12mg/dl in females will be included 2.Participants aged between 30-60 years will be included

Exclusion criteria

Exclusion criteria: 1.Participants with secondary Gout, pre diagnosed cases of Rheumatoid Arthritis. 2.Participants taking other medication for hyperuricemia. 3.Severe Systemic illness such as Chronic Kidney Disease, Diabetes Mellitus. 4.Chronic Cardiac Disease. 5.Pregnant women and lactating mother. 6.Participants having completed any other trial with in past 6 months. 7.Participants intaking alcohol

Design outcomes

Primary

MeasureTime frame
Serum Uric acidTimepoint: Before After and Follow up 0th, 31st, 45th

Secondary

MeasureTime frame
Subjective Parameters Tenderness Pain AmaTimepoint: Before after & on Follow up 0th, 31st, 45th

Countries

India

Contacts

Public ContactDr PV GIRI

Vaidyaratnam Ayurveda College, Ollur

doctorviswagiri@gmail.com9447527366

Outcome results

None listed

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