Effect of Enteral Nutrition Rich in Eicosapentaenoic Acid (EPA) on Patients Receiving Chemotherapy for GI Tumor
Gastric Cancer, Colorectal Cancer, Chemotherapy
About this trial
This is an interventional treatment trial for Gastric Cancer focused on measuring gastric cancer, colorectal cancer, chemotherapy, eicosapentaenoic acid, enteral nutrition
Eligibility Criteria
Inclusion Criteria:
- The cases have undergone radical excision on gastric cancer or colorectal cancer.
- Without contraindication for chemotherapy.
- Eligible for postoperative adjuvant XELOX chemotherapy.
- Capable of taking in food or drug orally.
- Without severe absorption dysfunction
- Able and willing to give written, informed consent
Exclusion Criteria:
- Comorbidities: diseases of hematology or immunology system; hepatic or renal dysfunction; metabolic diseases.
- BMI>35kg/m2
- Life expectancy≤3mo
- The chemotherapy treatment is palliative.
- The patient has received radiotherapy or neoadjuvant chemotherapy prior to the operation.
Sites / Locations
- First Affiliated Hospital, Sun Yat-sen UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Placebo Comparator
Experimental
Experimental
EN
ENLDEPA
ENHDPEA
The subjects take in 150g of Nutriall per day. Oral administration of the liquid is divided into 3 times per day. The treatment lasts for 21d. During the test period patients are treated with the first course of XELOX.
The subjects take in the same dose of Nutriall for the same duration as those in EN group. In addition, they take in 3 grams of EPA per day during the 21 days of treatment. The patients are treated with the first course of XELOX.
The subjects take in the same dose of supportan for the same duration as those in EN group. In addition, they take in 6 grams of EPA per day during the 21 days of treatment. The patients are treated with the first course of XELOX.