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

Phase 1
Conditions
Health Condition 1: M109- Gout, unspecified
Registration Number
CTRI/2023/06/053846
Lead Sponsor
Dr Gunjana Bhardwaj
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
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

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

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To decrease the symptoms of the affected joint as mentioned below <br/ ><br>1. Joint pain <br/ ><br>2. Stiffness <br/ ><br>3. Swelling <br/ ><br>4. Reddish blackish discoloration of skin <br/ ><br>5. Burning sensationTimepoint: 90 days
Secondary Outcome Measures
NameTimeMethod
To achieve normal serum uric acid & CRP levelsTimepoint: 90 days
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