MedPath

Evaluation of oral nano-silymarin formulation effect in prevention of liver damage induced by doxorubicin-cyclophosphamide chemotherapy regimen in patients with non-metastatic breast cancer

Phase 3
Recruiting
Conditions
on-metastatic breast cancer.
Malignant neoplasm of breast
Registration Number
IRCT20200408046990N13
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
70
Inclusion Criteria

Age between 18-65 y
Patients with diagnosis of non-metastatic breast cancer who will be treated by doxurobicin after mastectomy
Signing the written consent

Exclusion Criteria

Viral hepatitis
History of hypersensitivity to silymarin or similar compounds
Pregnancy and lactation
Any kind of liver injury resulting in rise of liver enzymes or bilirubin to higher than upper limit normal
Renal failure
Concomitant use of heptotoxic agents or antioxidants

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath