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Investigating the effect and safety of Lapis judaicus on kidney stones

Comparison of safety and efficacy of Lapis judaicus versus hydrochlorothiazide in patients with renal stones: a randomized clinical trial.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190413043264N1
Enrollment
75
Registered
2019-08-18
Start date
2019-07-05
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

renal stone. XIV Diseases of the genitourinary system

Interventions

Intervention 1: Intervention group A:Two capsules containing Lapis judaicus 1 gram for 2 months . Intervention 2: Intervention group B
Two capsules containing Lapis judaicus 1 gram +12.5 mg of hydrochlorothiazide for 2 months. Intervention 3: Control group C: Two capsules containing 12.5 mg of hydrochlorothiazide for 2 months.

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Have informed and written consent to participate in the study. Opaque stone greater than or equal to 5 mm and less than or equal to 10 mm. Age of 18 to 65 years of both sexes.Male and female. Satisfaction with the non-use of non-protocol treatments In one Last month, there was no effective drug on renal stone.

Exclusion criteria

Exclusion criteria: Pregnancy or lactation Sensitization to drugs of intervention Sensitization to sulfur Symptoms of digestive, liver or kidney, heart disease · · Obstruction or other emergency problem during intervention Dissatisfaction with the patient to continue the plan for both Organic disease (kidney, liver, heart disease, cancer, diabetes) Smoking, alcohol and substance abuse Coagulopathy disease Kidney transplant or single kidney.

Design outcomes

Primary

MeasureTime frame
Renal stone size. Timepoint: 2 Months. Method of measurement: KUB Sonography.

Secondary

MeasureTime frame
BUN. Timepoint: Before and after intervention. Method of measurement: DIRUI Automatic Analyzer.;Cr. Timepoint: Before and after intervention. Method of measurement: DIRUI Automatic Analyzer.;Calcium. Timepoint: Before and after intervention. Method of measurement: DIRUI Automatic Analyzer.;Aspartate Aminotransferase (AST). Timepoint: Before and after intervention. Method of measurement: DIRUI Automatic Analyzer.;Alanine Aminotransferas(ALT). Timepoint: Before and after intervention. Method of measurement: DIRUI Automatic Analyzer.;Urinalysis. Timepoint: Before and after intervention. Method of measurement: refractometry, microscopic and macroscopic urinalysis.;24- hour urine calcium. Timepoint: Before and after intervention. Method of measurement: DIRUI Automatic Analyzer.;24- hour urine magnesium. Timepoint: Before and after intervention. Method of measurement: DIRUI Automatic Analyzer.;24 -Hour urine citrate. Timepoint: Before and after intervention. Method of measurement: DIRUI Automatic Analyzer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElham Akbarzadeh

Shiraz University of Medical Sciences

akbarzadeh_e@sums.ac.ir+98 71 3234 5145

Outcome results

None listed

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