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Curcumin in the prevention of cisplatin-induced acute nephrotoxicity

Curcumin in the prevention of cisplatin-induced acute nephrotoxicity: a randomized,double-blind, placebo-controlled ?clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180722040556N8
Enrollment
100
Registered
2022-02-04
Start date
2022-02-20
Completion date
Unknown
Last updated
2022-02-07

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

Conditions

Nephrotoxicity. Other acute kidney failure

Interventions

Intervention 1: Intervention group: Patients with malignancy who will receive cisplatin with the dose 50-100 mg/m2 will be identified and after signing the consent will be considered for intervention

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Creatinine Clearance higher than 45 mL/min based on CKD-EPI (Chronic Kidney Disease Epidemiology Collaboration) The patient who will have enough compliance and ability to take curcumin orally. All adult cancer 's patients who will receive a regimen contains cisplatin (with the usual recommended dose between 50-100 mg / m2 )

Exclusion criteria

Exclusion criteria: Patients with active infection or symptoms of sepsis. Patients who have received nephrotoxic drugs such as aminoglycoside, amphotericin, vancomycin, colistin, media contrast, calcineurin inhibitors or Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) for the past 72 hours. Patients who are taking ifosfamide in their chemotherapy regimen Patients who are taking fluvoxamine, anagrelide, or hydroxy progesterone in their treatment regimen. Patients who may experience complications or allergic reactions to curcumin during treatment. Patients who had a history of acute kidney injury ( AKI ) before entering the study. Patients with bilirubin above 2 mg / dl or liver enzymes above 2.5 times the normal level.

Design outcomes

Primary

MeasureTime frame
Incidence of cisplatin-induced renal injury according to cheng in Glomerular Filtration Rate (GFR). Timepoint: Measurement of BUN, creatinine, in urine and serum at the time of the previous day, a day and five days after treatment with Cisplatin. Method of measurement: Measurement of urine and serum values by electrolyte analyzer and fordata analysis using Statistical Package for Social Sciences (SPSS).

Secondary

MeasureTime frame
The effect of curcumin on cisplatin-induced renal injury according to cheng in exertion rate of sodium. Timepoint: Measurement of sodium in urine and serum at the time of the previous day, a day and five days after treatment with Cisplatin. Method of measurement: Measurement of urine and serum values by electrolyte analyzer and fordata analysis using Statistical Package for Social Sciences (SPSS).;The effect of curcumin on cisplatin-induced renal injury according to cheng in exertion rate of potassium. Timepoint: Measurement of potassium in urine and serum at the time of the previous day, a day and five days after treatment with Cisplatin. Method of measurement: Measurement of urine and serum values by electrolyte analyzer and fordata analysis using Statistical Package for Social Sciences (SPSS).;The effect of curcumin on cisplatin-induced renal injury according to cheng in exertion rate of magnesium. Timepoint: Measurement of magnesium in urine and serum at the time of the previous day, a day and five days after treatment with Cisplatin. Method of measurement: Measurement of urine and serum values by electrolyte analyzer and fordata analysis using Statistical Package for Social Sciences (SPSS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzade Moghaddas

Esfahan University of Medical Sciences

moghaddas@pharm.mui.ac.ir+98 31 3792 7074

Outcome results

None listed

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