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Use of Cystone polyherbal extract in treatment of kidney Stone.

A Comparative clinical study to evaluate the Efficacy and Safety Of two Cystone formulations for treatment of Renal Calculi.

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2012/04/002544
Enrollment
60
Registered
2012-04-04
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Renal stones

Interventions

Intervention1: Cystone Extract Route Tablet: 1 tablet orally twice a day with meals for 12 weeks Control Intervention1: Cystone tablet: 2 tablets orally twice a day with meals for 12 weeks

Sponsors

The Himalaya Drug Company
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either gender with age 18-75 years (Both inclusive) 2. Patients with Renal calculi, diagnosis confirmed by X-ray KUB 3. Size of the calculi ranging from 04 mm - 09 mm 4. Able and willing to give written informed consent and comply with the requirements of the study protocol 5. Patients of reproductive potential (males and females) willing to use a reliable means of contraception (e.g hormonal contraceptive patch, intrauterine device and physical barrier) throughout study participation

Exclusion criteria

Exclusion criteria: 1. Patients having severe acute renal colic. 2. Any systemic disease requiring other medications or requiring surgery for calculus condition. 3. Complicated cases of Renal Calculi requiring surgical intervention, any condition chronic or current infectious disease such as but not limited to chronic renal infection including active urinary tract infection. 4. Known uncontrolled diabetes mellitus (DM), hypertension (HT), symptomatic congestive heart failure (CHF), unstable angina pectoris, myocardial infarction (MI) 5. Any other known urogenital disorders. 6. Known liver dysfunction, defined as total bilirubin >1.5 x the upper limit of Normal, (ULN) aspartate aminotransferase (AST/SGOT) > 2.5 x ULN, or alanine aminotransferase (ALT/SGPT) >2.5 x ULN Kidney disease, including serum creatinine level >1.5 x ULN 7. Subjects on herbal supplements for renal stone disease (plant extracts preparations or herbal medicines etc.) within previous 3 months. 8. Participated in another clinical drug trial within 3 months before recruitment. 9. Pregnancy or breast feeding 10. Evidence of significant uncontrolled concomitant disease which in the Investigators opinion would preclude patient participation 11. Currently active alcohol or drug abuse or history of alcohol or drug abuse within 24 weeks prior to baseline Patients with psychiatric illness or other condition that would limit compliance with study requirements 12. Patients receiving or has received any investigational drug within 30 days before receiving the first dose of study medication 13. Subjects who refuse to sign the informed consent document.

Design outcomes

Primary

MeasureTime frame
Reduction in the stone size (in mm) or the expulsion of stoneTimepoint: day 30 day 60 and day 90

Secondary

MeasureTime frame
Painless expulsion of calculi fragments: Reduction in pain: Consumption of Analgesics:Timepoint: day 30, day 60 and day 90

Countries

India

Contacts

Public ContactDr Pralhad Patki

The Himalaya Drug Company

dr.patki@himalayahealthcare.com08023714444

Outcome results

None listed

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