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A Clinical trial to study the effectiveness of Laghumanjishthadi kwath in the management of Vatarakta(Gout)

A Clinical study on the efficacy of polyherbal compound in the management of Vatarakta(Gout)

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/053846
Enrollment
60
Registered
2023-06-14
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

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 Gunjana Bhardwaj
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients presented with classical symptoms of Vatarakta as mentioned in classical texts (joint pain, swelling, stiffness, reddish blackish discoloration of skin and burning sensation) 2.Raised serum uric acid levels more than 7 mg/dl 3.People of both sexes all socioeconomic conditions and ethnicity 4.Patients willing to participate in the study

Exclusion criteria

Exclusion criteria: 1.Age less than 30 years and more than 70 years 2.Presence of complications of systemic illnesses like nephropathy chronic liver disease 3.Presence of diseases like Carcinoma HIV malignant hypertension uncontrolled diabetes 4.Presence of other joint illnesses like osteoarthritis rheumatoid arthritis SLE 5.Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
To decrease the symptoms of the affected joint as mentioned below 1. Joint pain 2. Stiffness 3. Swelling 4. Reddish blackish discoloration of skin 5. Burning sensationTimepoint: 90 days

Secondary

MeasureTime frame
To achieve normal serum uric acid & CRP levelsTimepoint: 90 days

Countries

India

Contacts

Public ContactDr Ranjan Kalita

Government Ayurvedic College and Hospital Guwahati

gunjana12345@gmail.com7217869308

Outcome results

None listed

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