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Effect Of Kasmaryadi Kashaya In The Management of Elevated Serum Uric acid level.

Phase 2
Conditions
Health Condition 1: E790- Hyperuricemia without signs of inflammatory arthritis and tophaceous disease
Registration Number
CTRI/2024/07/069896
Lead Sponsor
I
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1) Subjects in the age group between 18-60 years having elevated Serum uric acid

level above 6.8 mg/dL.

2) Subjects irrespective of gender and socio-economic status.

3) Subjects who are willing to sign the consent form.

Exclusion Criteria

1) Pregnant and lactating women.

2) Subjects with known cases of Malignancy, Diabetes mellitus, any Concurrent

Hepatic disorders, Chronic Renal failure, Hyperthyroidism and Hypothyroidism

3) Subjects on medication with aspirin (low dose 1-2 g per day), beta blockers and

alpha -1 blockers for hypertension, antidepressants, modern diuretics and on

medication of hyperuricemia.

4) Known alcoholic subjects and subjects consuming high purine diet.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.To study the efficacy of Kasmaryadi Kwatha in the management of Hyperuricemia <br/ ><br>2.To assess the efficacy of Kasmaryadi Kwatha in reducing symptoms of symptomatic <br/ ><br>patients using Brief Pain Inventory Scale and in improving quality of life assessed by <br/ ><br>Bengali version of Questionnaire assessing impact of hyperuricemia on quality of lifeTimepoint: 1.Serum Uric acid test. <br/ ><br>2.Pain (Assessed by brief pain inventory scale) <br/ ><br>3.Quality of life (Assessed by Bengali version of questionnaire assessing impact of <br/ ><br>hyperuricemia on quality of life). <br/ ><br> <br/ ><br>Assessment will be done on 0th day, 8th day, 16th day and 31st day
Secondary Outcome Measures
NameTimeMethod
To assess the safety of Kasmaryadi Kwatha in subjects diagnosed with Hyperuricemia. <br/ ><br>Timepoint: Liver Function Test,Renal Function Test,Random Blood Sugar and Blood Routine Examination with ESR will be done on 0th and 16th day to assess safety
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