Clinical Trial Finder

Inclusion Criteria:

• - 18 years or older.

• - Primary colon adenocarcinoma.

• - Curative operation is possible.

• - Patient has a life expectancy of at least 12 months.

• - Patient signs the informed consent and agrees to attend all study visits.

Exclusion Criteria:

• - Recurrent colon adenocarcinoma.

• - Metastatic disease.

• - Cancer that will require multiorgan resection.

• - Pregnant or suspected pregnancy.

• - Patient with a comorbid illness or condition that would preclude the use of surgery (ASA 5).

• - Patients with concurrent or previous malignant tumors within 5 years before the study enrollment.

• - Patient undergoing emergency procedures.

• - Dialysis.

• - Liver dysfunction, child pugh B or worse.

• - NRS score <2 or >5.

• - BMI under 18.5.

• - Weight loss 15% or more past 6 months.

• - Serum albumin less than 30 without liver or renal dysfunction.

• - Chronic malnutrition: short bowel syndrome, previous gastrectomy, pancreatic dysfunction.

- Language barrier or other reasons why informed consent is not possible

The hypothesis in this study are: 1. Perioperative ONS decreases surgery related morbidity. 2. Perioperative ONS increases the quality of life after surgery. 3. Perioperative ONS decreases the length of stay in institutional care. 4. Perioperative ONS decreases 90-day mortality and improve 5-year survival. 5. Perioperative ONS benefits the patients to tolerate the adjuvant chemotherapy with less side effects. 6. Perioperative ONS protects patients from postoperative nutritional depletion. Primary end point is to investigate whether the preoperative oral nutritional support decreases the number of complications during the 30-day follow up after the surgery. Secondary end points are to study the effect of oral nutritional support on quality of life after surgery, length of hospital stay, disease free and overall survival. Randomization: Patients having a surgery for adenocarcinoma of the colon are randomized on their preoperative visit in the outpatient clinic about 2-3 weeks prior to surgery. The patients are randomized in two different groups according to NRS-2002 results. Both groups contain equal number of patients with normally nourished patients (NRS-2002 1-2) and malnourished patients by NRS 3 or more. NRS >5 patients are excluded (nutritional support is recommended before the surgery). The control group (group 1) will continue their regular diet. The study group (group 2) will get preoperative nutritional support two weeks before the operation and the nutritional support will continue 10 days after the operation. The control group will continue their regular diet after the operation. Thus the randomization groups will be (total number of patients 318): 1. no oral nutritional support (control group) n=159. 2. pre and postoperative oral nutritional support (intervention group) n=159. Preoperative assessment and data-collection: All patients attending this study have a visit in the out-patient clinic 2-3 weeks prior the surgery. The height and weight are measured at the baseline. 3 and 6 months previous weights recalled by patient. ASA (The American Society of Anesthesiologists) classification is estimated by anesthesiologist. Whole body computer tomography is done to assess the possibility of metastases or locally spread cancer. Laboratory markers including total blood count, CRP (C-reactive protein) , creatinine, sodium, potassium, albumin, prealbumin, HbA1c, CEA (Carcinoembryonic antigen), transferrin and lipids (LDL, HDL, triglycerides) concentration are measured. History of smoking, alcohol consumption and other diseases and medications are recorded. NRS-2002 questionnaire is filled, as well as QoL- questionnaire and exercise questionnaire. Bioelectrical impedance analysis (InBody) and handgrip strength are measured. Laboratory parameters, as described above, are measured at the time of randomization, at admission to hospital on the morning of surgery, leaving the hospital and about 1 and 3 months and 1,2 and 5 years after surgery. BMI, hand grip strength, bioelectrical impedance analysis are collected and the patients fill the QoL-questionnaire and exercise questionnaire at the same time points. The side effects of chemotherapy are monitored, as well as discontinuation of chemotherapy. Complication form will be filled when necessary. Follow- up: Follow-up will be same as other colon cancer patients. The follow.up will continue 5 years and the only difference is 3 month phone call. Patients will also fill exercise and quality of life forms and bioimpedance and handgrip strength will be measured. First follow up visit after the surgery is at the outpatient clinic 1 month after the surgery. At that time patient is interviewed about recovery from surgery, patients who went to health care center to recover from surgery are asked about the length of stay and possible complications after leaving the hospital. The patients´ fill the 4-day food diary, exercise questionnaire and QoL questionnaire (RAND-36). The blood samples are taken. Bioelectrical impedance analysis and handgrip strength are measured as well. Second follow up at 3 months after the surgery is by phone. Then the recovery from surgery is checked, as well as patients are asked to keep 4-day food diary. The blood samples are collected. Patients fill quality of life and exercise questionnaire. Patients have CEA, hemoglobin, leucocyte count and thrombocyte count measured every 3 months until 2 years, and every 6 months until 5 months on a routine basis. Whole body CT scan is done in a year after the surgery. There are also follow up CT scans at the oncology clinic on patients who receive adjuvant therapy. They will be utilized for analysis on recovery from the sarcopenia and its effect on survival and toxicity of chemotherapy. There are routine hospital visits 1,2 and 5 years after the surgery. Laboratory parameters, BMI, bioelectrical impedance analysis and handgrip strength are measures at each visit. The patients fill the QoL questionnaire and exercise questionnaire also at each time points. charlson comorbidity index and who classification are also marked.

Arms

Active Comparator: regular diet

The control group (group 1) will continue their regular diet.

Active Comparator: nutritional support Resource 2.5

The intervention group (group 2) will get preoperative nutritional support two weeks before the operation and the nutritional support will continue 10 days after the operation.

Interventions

Dietary Supplement: - regular diet

The control group (group 1) will continue their regular diet.

Dietary Supplement: - nutritional support Resource 2.5

The intervention group (group 2) will get preoperative nutritional support (Resource 2.5 Compact/fibre combact) two weeks before the operation and the nutritional support will continue 10 days after the operation.