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Cystone in kidney stones

Phase 3
Conditions
Health Condition 1: null- urolithiasis
Registration Number
CTRI/2012/01/002350
Lead Sponsor
The Himalaya Drug
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

?Subject with Urolithiasis as disgnosed by clinically as well as ultrasonographically with calculi measuring more than 5 mm.

?Hematologic and Biochemical parameters within normal limits.

? Willing to sign inform consent document

Exclusion Criteria

?Those with serious cardiovascular, cerebrovascular, respiratory, liver or renal disease or any other disorder.

?The subjects not to have used any drugs, for at least 1 week prior to the study.

?Subjects with a strong history of food or drug allergy of any kind.

?Subjects not to have been on weight reducing diets within 3 months prior to the start of the study.

?No other drugs (including aspirin) to be ingested during the course of the study.

?Patients unwilling to provide informed consent or abide by the requirements of the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
symptomatic relief from clinical symptoms of urolithiasis and reduction in the stone size by ultrasonographyTimepoint: 3 months
Secondary Outcome Measures
NameTimeMethod
To assess the safety profile of Cystone Extract route tablet in Urolithiasis and overall compliance to the drug treatment. <br/ ><br>Timepoint: At monthly intervals for the period of 3 months
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