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Clinical Trials/NCT00868400
NCT00868400
Completed
Not Applicable

Multi-centre Double-blind Randomized Trial of the Clinical Value of Preoperative Oral Carbohydrate Loading in Colorectal Surgery.

Gulhane School of Medicine1 site in 1 country215 target enrollmentMay 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Colorectal Disorders
Sponsor
Gulhane School of Medicine
Enrollment
215
Locations
1
Primary Endpoint
Overall 30-day complication rate
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The aim of this study is to provide conclusive clinical evidence as to whether or not the preoperative administration of oral carbohydrate-rich solutions is effective on the outcomes of patients undergoing colorectal surgery.

Detailed Description

Preoperative oral carbohydrate loading is an issue that has been investigated extensively in terms of its fundamental and biochemically apparent effects and potential benefits. Most commonly, proponents of the application advocate that it may be beneficial for improving patient outcomes and for decreasing complication rate by attenuating postoperative insulin resistance. To date, however, no study with a sufficient sample size has been able to demonstrate that it has a marked value in clinical practice. Almost all of the clinical benefits ascribed to the application have been based on subjective well-being, which can also be provided with non specific simple beverages. A study conducted to show whether or not the application has direct influence on patient outcome, therefore, could significantly contribute insights on this topic. The present study was planned to consist of three study arms, namely: 1.Study group, which will be given high-carbohydrate beverage (Nutricia preOp®, Numico, Zoetermeer, The Netherlands) 2. Placebo group, which will be given flavored water, and 3. Control group (surgery after overnight fast). The revised power analysis shows that an accrual of 74 patients in each group would allow detecting a 15% difference in the rate of complications with 80% power at the 5% level of significance (two tailed). We hope we will have recruited at least 220 subjects at the end of a two-year course. Once the data recording is complete, this study will be the largest one ever conducted to investigate this topic.

Registry
clinicaltrials.gov
Start Date
May 2009
End Date
May 2012
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Gulhane School of Medicine
Responsible Party
Principal Investigator
Principal Investigator

Mehmet Fatih Can

Associate Professor

Gulhane School of Medicine

Eligibility Criteria

Inclusion Criteria

  • patients undergoing colorectal surgery for malignant or benign diseases

Exclusion Criteria

  • disorders that prolongs gastric emptying
  • existence of an increased risk for aspiration of gastric content
  • anal surgery (haemorrhoidectomy, fistulotomy...etc)
  • emergency operations

Outcomes

Primary Outcomes

Overall 30-day complication rate

Time Frame: 2 years

Secondary Outcomes

  • Length of intensive care unit and hospital stay(2 years)
  • Overall 30-day mortality rate(2 years)
  • Patient recovery(2 years)
  • Patient discomfort(2 years)
  • need for insulin infusion(2 years)

Study Sites (1)

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