Skip to content

Evaluating the effect of atorvastatin on kidney stone.

Evaluating the effect of atorvastatin on metabolic abnormalities, Tubular injury and oxidative stress in recurrent calcium stone patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017021826406N2
Enrollment
30
Registered
2017-06-17
Start date
2016-05-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Calcium kidney stone. Calculus of kidney

Interventions

Intervention 1: Intervention group: Patients taking atorvastatin oral tab (20 mg). Duration and Dosage: One daily for 3 month. Intervention 2: Control group: Patients taking placebo. Duration and Dosa
Treatment - Drugs
Placebo
Intervention group: Patients taking atorvastatin oral tab (20 mg). Duration and Dosage: One daily for 3 month.
Control group: Patients taking placebo. Duration and Dosage: One daily for 3 month

Sponsors

Urology and Nephrology Research Center, Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: History of calcium kidney stone (stone should be radio-opaque in radiological evaluation); at least 2 times of kidney stone episodes (Recurrent stone); at least 20 days since the last treatment; age 18 to 65 years; Hyperoxaluria (24-hour urine oxalate over 40 and less than 80 mg); willingness to cooperate in the study. Exclusion criteria: Primary or enteric hyperoxaluria (urine oxalate>80 mg/24h);taking any drugs or supplements with antioxidant or anti-inflammatory effects (e.g. steroids, Nonsteroidal Antiinflammatory Drugs, pioglitazone, …), multivitamins containing vitamin A,C or E and any supplement containing anti-oxidants; History of diabetes mellitus, hepatic failure, thyroid or parathyroid diseases, cancers or immunologic diseases, chronic kidney disease (Glomerular filtration rate< 60), Urinary tract infection and chronic diarrhea; Pregnancy or lactation

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Urine malondialdehyde. Timepoint: Before the intervention, 3 months after the intervention. Method of measurement: colorimetric method using Thiobarbituric acid.;Urine neutrophil gelatinase-associated lipocalin. Timepoint: Before the intervention, 3 months after the intervention. Method of measurement: ELISA.

Secondary

MeasureTime frame
Morning urine pH. Timepoint: Before the intervention,3 months after the intervention. Method of measurement: Dip stick.;24 hour urine volume. Timepoint: Before the intervention,3 months after the intervention. Method of measurement: observation.;24 hour urine creatinine. Timepoint: Before the intervention,3 months after the intervention. Method of measurement: Colorimetric.;24 hour urine calcium. Timepoint: Before the intervention,3 months after the intervention. Method of measurement: Colorimetric.;24 hour urine oxalate. Timepoint: Before the intervention,3 months after the intervention. Method of measurement: Assay kit with Enzymatic method.;24 hour urine phosphorus. Timepoint: Before the intervention,3 months after the intervention. Method of measurement: Colorimetric.;24 hour urine magnesium. Timepoint: Before the intervention,3 months after the intervention. Method of measurement: Colorimetric.;24 hour urine citrate. Timepoint: Before the intervention,3 months after the intervention. Method of measurement: Assay kit with Enzymatic method.;24 hour urine uric acid. Timepoint: Before the intervention,3 months after the intervention. Method of measurement: Colorimetric.;24 hour urine sodium. Timepoint: Before the intervention,3 months after the intervention. Method of measurement: flame photometry or indirect ion selective electrode.;24 hour urine potassium. Timepoint: Before the intervention,3 months after the intervention. Method of measurement: flame photometry or indirect ion selective electrode.;24 hour urine chloride. Timepoint: Before the intervention,3 months after the intervention. Method of measurement: flame photometry or indirect ion selective electrode.;Calcium oxalate relative supersaturation. Timepoint: Before the intervention,3 months after the intervention. Method of measurement: calculation by lithorisk software.;Calcium phosphate relative supersaturation. Timepoint: Before the intervention,3 months after the intervention. Method of measurement: c

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSanaz Tavasoli

Urology and Nephrology Research Center

s.tavasoli@sbmu.ac.ir; sanaz.tavasoli@gmail.com+98 21 2256 7222

Outcome results

None listed

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