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Effect of atorvastatin in prevention of aminoglycosids-induced nephrotoxicity

Atorvastatin efficacy on prevention of aminoglycosids-induced nephrotoxicity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201301283449N11
Enrollment
50
Registered
2013-03-02
Start date
2013-09-23
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

Acute Kidney Injury. previously called acute renal failure (ARF), is a rapid loss of kidney function.

Interventions

Intervention 1: Atorvastatin 40 mg Tab as daily during antibiotic therapy. Intervention 2: Placebo of atorvastatin as daily in all period of antibiotic therapy.
Prevention
Placebo
Atorvastatin 40 mg Tab as daily during antibiotic therapy.
Placebo of atorvastatin as daily in all period of antibiotic therapy

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients who are candidates for treatment with an aminoglycoside (gentamicin or amikacin) and at least 5 days in this study will receive antibiotics. Exclusion criteria ((Exclusion criteria: - Patients aged less than 18 or more than 65 years. - A history of kidney problems ((GFR <60ml/min - Concurrent use of other nephrotoxic drugs -Concomitant use of other drugs, antioxidants and nephroprottectivev - Patients who have contraindications to statins (hypersensitivity to the drug or drug formulation, active liver disease, unexplained and persistent increase in serum aminotransferases, pregnancy)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
NGAL. Timepoint: A urine sample of the patients at baseline, 24 hours after starting treatment and at end of treatment period will be collected. Method of measurement: ELISA KIT.;Renal Toxicity. Timepoint: As daily dvaluation. Method of measurement: Based on RIFEL Criteria.;Nitric Oxide. Timepoint: A blood sample from the patients will be collected at times 0, 24h and end of treatment period. Method of measurement: ELISA Kit.

Secondary

MeasureTime frame
Renal Function status. Timepoint: End of treatment. Method of measurement: Renal Function Tests.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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