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investigating the effect of atorvastatin on the cisplatin induced nephrotoxicity

investigating the effect of atorvastatin on the cisplatin induced nephrotoxicity in patients with solid tumors

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20140605017982N2
Enrollment
40
Registered
2020-06-05
Start date
2020-05-04
Completion date
Unknown
Last updated
2020-06-15

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

Conditions

Cisplatin nephrotoxicity. Acute kidney failure, unspecified

Interventions

Intervention 1: Atorvastatin( sobhan) 40 mg,1 hour before cisplatin administration then continue atorvastatin daily till 7 days after starting cisplatin. Intervention 2: Control group: placebo starts

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: New cases of patients with solid tumors under Cisplatin therapy, minimum age of 18 glomerular filtration rate( GFR) > 60 ml/min serum creatinine less than 1.5 mg/dl

Exclusion criteria

Exclusion criteria: Patients who used cisplatin less than 50mg/m2 or divided dose of cisplatin in several days patients with a past history of Cisplatin therapy, chronic kidney disease, NSAIDS usage or using any nephrotoxic drugs will not participate in this study patients with a history of NSAIDS usage or using any nephrotoxic drugs will not participate in this study patients with a historyof chronic kidney disease

Design outcomes

Primary

MeasureTime frame
Percentage of people with renal failure. Timepoint: measurement of blood Urea nitrogen, creatinine, potassium, magnesium before intervention and 8 and 21 days after intervention. Method of measurement: measurement of blood Urea nitrogen, creatinine, potassium, magnesium.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNasrin Namdari

Shiraz University of Medical Sciences

namdari_n@sums.ac.ir+98 71 3647 4301

Outcome results

None listed

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