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The efficacy of deferoxamine in preventing nephrotoxicity of anthracyclins in pediatric cancer patients

The efficacy of deferoxamine in preventing nephrotoxicity of anthracyclins in pediatric cancer patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016021915666N3
Enrollment
60
Registered
2016-08-28
Start date
2015-12-01
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

Nephropathy of Anthracyclins. Nephropathy induced by other drugs, medicaments and biological substances

Interventions

Intervention 1: Control group: no treatment. Intervention 2: Intervention group 1: Deferoxamine 10-20 mg/kg. Frequency and route of administration is once per day Iv infusion over 8 hours concomitant
Treatment - Drugs
Intervention group 1: Deferoxamine 10-20 mg/kg. Frequency and route of administration is once per day Iv infusion over 8 hours concomitant with the anthracyclin infusion .
Intervention group 2: Deferoxamine 50 mg/kg. Frequency and route of administration is once per day IV infusion over 8 hours.

Sponsors

Vice chancellor of research, Shiaz Univeisity of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 18 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: signing informed consent; male or female aged between 2-18 years at screening; new pediatric cancer patients who are going to receive Anthracyclin drugs as part of their chemotherapy regimen. Exclusion criteria: patients below two years old; patients with previous history of treatment with any kind of chemotherapy or radiotherapy; diagnosis of primary or metastatic renal tumors; patients with congenital or acquired renal problems

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Blood Urea Nitrogen. Timepoint: before and after chemotherapy coarse. Method of measurement: Photometric.;Serum creatinin. Timepoint: before and after chemotherapy coarse. Method of measurement: Photometric.;Urine N-acetyl beta glucoseaminidase. Timepoint: before and after chemotherapy coarse. Method of measurement: N-acetyl-beta-glucosaminidase assay.;Urine creatinin. Timepoint: before and after chemotherapy coarse. Method of measurement: Collection of 24 hours urine.;Urine protein. Timepoint: before and after chemotherapy coarse. Method of measurement: Collection of 24 hours urine.;Micro-albuminuria (Urine albumin-to-creatinine ratio). Timepoint: before and after chemotherapy coarse. Method of measurement: Immuno-turbidimetric.;Nephropathy sign. Timepoint: before and after chemotherapy coarse. Method of measurement: Sonograghy.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Reza Bordbar

Shiraz University of Medical Sciences

bordbarm@sums.ac.ir+98 71 3628 1563

Outcome results

None listed

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