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Observing the effect of nanocurcumin oral product in preventing cisplatin nephrotoxicity in cancer patients

Evalution of oral nano-curcumin formulation efficacy in prevention of cisplatin induced nephrotixicity in cancer patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200408046990N11
Enrollment
40
Registered
2022-10-08
Start date
2020-05-21
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Cancer.

Interventions

Intervention 1: Intervention group:in the intervention group, two 40mg synacorcumin capsules per day, made by Elixir Nano Sinat, are prescribed for six chemotherapy courses, and in the control group,

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients with cancer and candidates for chemotherapy with regimen containing cisplatin at a dose of 70mg/m2 every three weeks or 40mg/m2 weekly Patient age above 18 years and below 70 years GFR>60 ml/min At the start of chemotherapyNormal liver function Normality of patients' CBC

Exclusion criteria

Exclusion criteria: Allergy to curcuminPatient dissatisfactionReduction of patient's GFR below 45ml/min during treatmentReceiving other nephrotoxic drugs such as aminoglycosides, amphotericin, vancomycin Patients with chronic heart failure EF<60%Patients with untreated hypothyroidism or hyperthyroidismPatients with active infectionReceiving anti-inflammatory and antioxidant drugs at the same timeUnfavorable health status (PS<70%) based on karnofsky index

Design outcomes

Primary

MeasureTime frame
Serum ceratinine level, BUN. Timepoint: ?At the beginning of each chemotherapy course. Method of measurement: Blood test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSare Hosseini

Mashhad University of Medical Sciences

hosseinis@mums.ac.ir+98 51 3841 2081

Outcome results

None listed

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