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Clinical Trials/NCT02626195
NCT02626195
Completed
Not Applicable

Prospective Study of Preoperative Nutritional Support in Malnutritional Pancreatobiliary Cancer Patients

National Cancer Center, Korea1 site in 1 country50 target enrollmentOctober 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pancreatic Cancer
Sponsor
National Cancer Center, Korea
Enrollment
50
Locations
1
Primary Endpoint
postoperative complication
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Malnutrition patients are known to have more postoperative complications and mortality. And most of hepatobiliary-pancreatic cancer surgeries accompany high postoperative morbidity and mortality rate. Therefore for the malnourished patients anticipating major surgery, preoperative nutritional support is recommended according to the ASPEN (American society of parenteral and enteral nutrition) and ESPEN (European society of parenteral and enteral nutrition) guideline. However there is no prospective trial to prove the clinical impact of preoperative nutritional support for malnourished patients.

The purpose of this study is to evaluate the clinical impact of preoperative nutritional support for malnourished cancer patients anticipating HBP surgery. Primary objective is to compare the complication rate and secondary object is to compare the quality of life, hospital stay and cost.

Detailed Description

This is single arm study with historical comparison. The historical control group did not receiving nutritional support. In previous results show that about 25% complication rates. Complication rates are expected in the group receiving nutritional support is less than 10 % ( previous studies (NCCNCS-11-460)). For support group, preoperative nutritional support is given for 5 or more days preoperatively by nutritional support program. Nutritional support program is briefly described below. Interval: 5-10 days Contents: admission is required * Calories: 30-35Kg, via enteral or parenteral * Protein: 1.2-1.5g/Kg * Lipid : 1-1.5g/Kg * Mineral and vitamins supply * Blood glucose control * Daily monitoring by dietician and specialized nurse

Registry
clinicaltrials.gov
Start Date
October 2013
End Date
April 5, 2017
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sang-Jae Park

Head of Center for Liver Cancer, Chief of the Liver and Pancreatobiliary Cancer Branch

National Cancer Center, Korea

Eligibility Criteria

Inclusion Criteria

  • Subjects in anticipating major surgery of hepatobiliary pancreatic cancer
  • Patients diagnosed with malnutrition (at least more than one)
  • PG-SGA B or C
  • Weight loss \>10% within 6 month
  • Serum Albumin \<3.0
  • Age less than 80 years old over 20 years old
  • Performance status (ECOG scale): 0-1
  • Adequate organ functions
  • Hb ≥7.0 g/dl
  • ANC ≥1,500/mm3

Exclusion Criteria

  • Biopsy, drainage tube insertion, and other minor surgery
  • palliative surgery
  • Serious illness or medical conditions, as follows;
  • congestive heart failure (NYHA class III or IV)
  • unstable angina or myocardial infarction within the past 6 months,
  • significant arrhythmias requiring medication and conduction abnormality such as over 2nd degree AV block
  • uncontrolled hypertension
  • hepatic cirrhosis( ≥ Child class B)
  • interstitial pneumonia, pulmonary adenomatosis
  • psychiatric disorder that may interfere with and/or protocol compliance

Outcomes

Primary Outcomes

postoperative complication

Time Frame: at discharge. (expected the duration of hospital stay of postoperation is 4~6 weeks.)

expected the duration of hospital stay of postoperation is 4\~6 weeks.

Secondary Outcomes

  • quality of life(preoperative, postoperative 14days)
  • postoperative hospital stay(expected the duration of hospital stay of postoperation is 4~6 weeks.)
  • postoperative cost( + nutritional support cost)(at discharge. (expected the duration of hospital stay of postoperation is 4~6 weeks.))

Study Sites (1)

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