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A Clinical Study of Cystone GNX Tablet in Urolithiasis (Kidney stones)

Phase 2
Conditions
Health Condition 1: N209- Urinary calculus, unspecified
Registration Number
CTRI/2017/08/009545
Lead Sponsor
The Himalaya Drug Company
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1. Subject with Urolithiasis as diagnosed by clinically and ultrasonographically with calculi measuring 5-10mm.

2. Subjects aged between 18-50 years of either sex.

3. Hematologic and Biochemical parameters within normal limits.

4. Willing to sign inform consent document and follow study procedures.

Exclusion Criteria

1.Subjects with severe obstructive uropathy,

2.Subjects with serious systemic medical disorder,

3.Subjects not to have used any drugs for at least 1 week prior to the study,

4.Subjects with a strong history of food or drug allergy,

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

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

7.Pregnant and lactating women

8.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
Secondary Outcome Measures
NameTimeMethod
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