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The efficacy of deferoxamine to prevent hepatic fibrosis in children being treated with Anthracyclins

Phase 3
Conditions
Hepatic fibrosis.
Hepatic fibrosis
Registration Number
IRCT2016080315666N4
Lead Sponsor
Vice chancellor of research, Shiaz Univeisity of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
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 metastatatic hepatic tumors, chronic liver disease and liver cirrhosis.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
iver function test. Timepoint: before and after chemotherapy coarse. Method of measurement: hematology analysis.;Hyaluronic acid. Timepoint: before and after chemotherapy coarse. Method of measurement: FDM analysis kit.;Gamma-microglobulin. Timepoint: before and after chemotherapy coarse. Method of measurement: hematology analysis.;Liver fibrosis. Timepoint: before and after chemotherapy coarse. Method of measurement: liver fibroscan.;Liver dysfunction signs. Timepoint: before and after chemotherapy coarse. Method of measurement: Sonograghy.
Secondary Outcome Measures
NameTimeMethod
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