CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted
Drug / intervention
Oral Impact (preoperative enteral nutritional supplement)drug
Likely dose
Not stated in record
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Search/NCT00247793
NCT00247793N/ACompleted

The Effect of Pre- and Postoperative Supplemental Enteral Nutrition in High-Risk Patients Undergoing Elective Cardiac Surgery. A Prospective Double Blind Study.

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)·interventional·Posted Nov 2, 2005·Updated Nov 2, 2005

In Brief

A clinical study evaluating Oral Impact (preoperative enteral nutritional supplement) for Thoracic Surgery and 2 related conditions. Completed, across 1 site.

Detailed Summary

Effect of two preoperative oral immune-enhancing nutritional supplements in patients at high risk of infection after cardiac surgery: a randomized placebo-controlled study. Introduction: In our first study we showed that the use of a preoperative oral immune-enhancing nutritional supplement (OIENS) resulted in an improved patients' host-defence with a reduction in postoperative infectious morbidity in 'high-risk' cardiac surgery patients. The use of the OIENS resulted also in less postoperative organ dysfunction. Experimental studies have shown that additional glycine results in less ischemia-reperfusion damage and that glycine has anti-inflammatory properties. Objective: The use of an OIENS in the preoperative period in patients at high risk of infection after elective cardiac surgery with the use of cardiopulmonary bypass (CPB) results in a reduction in infections as in our first study. The addition of 9.6 gram glycine per sachet OIENS results in a further reduction in postoperative dysfunction. Design: A prospective randomized placebo controlled study with two oral immune enhancing nutritional formula's and an isocaloric control formula. Patients: Seventy-four consecutive patients undergoing cardiac surgery with the use of an CPB who met one or more of the following inclusion criteria: Age 70 years or older, mitral valve replacement or cardiac ejection fraction less then 40%. Exclusion criteria were age \< 18 years, proven malignancy, use of corticosteroids, severe renal and liver failure. Definition of a protocol violation was the intake of less then 5 L or more then 10 L of the nutritional supplement in the preoperative period. Intervention: Patients were split up in three groups by concealed randomisation. One group received the arginine, omega3-PUFAs and nucleotides enriched formula (OIENS). Another group received the OIENS further enriched with glycine (OIENS+glyc). The control group received an isocaloric nutritional supplement without the enrichments.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesNetherlands
Collaborators--

Timeline

N/ACompletedFinished
19961997199819992000200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedNov 2, 2005
Enrollment StartJul 1, 1996
Study CompletionDec 1, 1998
TodayJul 2, 2026
Posted 20.7 years ago

Interventions

Oral Impact (preoperative enteral nutritional supplement)drug