Last updated: December 19, 2023
Sponsor: Tanta University
Overall Status: Active - Recruiting
Phase
3
Condition
Colorectal Cancer
Metastatic Cancer
Treatment
Silymarin
Clinical Study ID
NCT05631041
Silymarin in Colorectal Cancer
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patients with histologically and/or radiologically confirmed diagnosis of metastaticcolorectal carcinoma.
- Patients who received FOLFOX or XELOX as first line chemotherapy
- Both genders.
- Age ≥18 years old.
- Performance status 0-1 according to the Eastern Cooperative Oncology Group (ECOG).
- Patients with adequate hematologic parameters (white blood cell count ≥3000/mm3, granulocytes ≥1500/mm3, platelets ≥100,000/mm3, hemoglobin ≥ 8 gm/l).
- Patients with adequate renal functions (serum creatinine ≤1.5 mg/dL).
- Patients with adequate hepatic functions (bilirubin ≤1.5 mg/dL or albumin ≥3 g/dL).
Exclusion
Exclusion Criteria:
- Patients with active liver diseases (chronic viral hepatitis, autoimmune hepatitis,alcoholic hepatitis, Wilson's disease, hemochromatosis, or cirrhosis).
- Patients with a history of other malignancy.
- Patients with brain metastasis.
- Patients with active infection.
- Patients with RAS wild type cancer.
- Patients on chronic use of corticosteroids.
Study Design
Total Participants: 64
Treatment Group(s): 1
Primary Treatment: Silymarin
Phase: 3
Study Start date:
December 31, 2022
Estimated Completion Date:
December 31, 2024
Study Description
Connect with a study center
faculty of Pharmacy , Tanta University
Tanta,
EgyptActive - Recruiting
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