KCT0005570
Not yet recruiting
未知
The effect of postoperative supplemental parenteral nutrition (SPN) in gastric cancer patients who underwent gastrectomy: A multicenter prospective randomized controlled trial
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Seoul National University Hospital
- Enrollment
- 224
- Status
- Not yet recruiting
- Last Updated
- 5 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •(1\) Patients who will undergo curative gastric cancer surgery (total gastrectomy, distal gastrectomy, proximal gastrectomy, and pylorus\-preserving gastrectomy)
- •(2\) A Malnourished patient who meets one or more of the following:
- •\- BMI \= 20\.5 kg/m2: BMI will be measured 1 day before surgery
- •\- Rapid weight loss (decreased by more than 5% in 2 months)
- •(3\) Patients over 18 years of age
- •(4\) Patients who are expected to receive PN for more than five days after surgery
- •(5\) Patients who are able to eat orally, but cannot fulfill the recommened calorie requirement by oral intake alone.
Exclusion Criteria
- •(1\) In case that the patients have already provided parenteral nutrition prior to the consent of the study (oral diet prior to consent has nothing to do with study)
- •(2\) In case that the patients need tube feeding
- •(3\) Patients who are contraindicated to parenteral nutrition: heart failure (if the patient has current symptoms or receiving heart failure treatment, if ejection fraction(EF) was less than 40% in preoperative echocardiogram), Child\-Pugh score C, renal failure (patient with 50% increased creatinine more than upper normal limit, patients currently undergoing renal replacement therapy), and pulmonary edema (appropriate chest X\-ray signs for pulmonary edema), and the patient who suffered from allergie reaction to parenteral nutrition solutions.
- •(4\) Patients who are not easily able to obtain venous pathways or are vulnerable to side effects due to venous pathways (e.g. increased infection risk due to immunosupressant status)
- •(5\) Vulnerable subject (those who lack the decision making ability, pregnant women, or women who are planning to conceive)
- •(6\) Other patients whom the investigator has determined to be inappropriate to participate in this study
Outcomes
Primary Outcomes
Not specified
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