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Trials / Completed

CompletedNCT00798447

Efficacy and Safety of a PN Regimen Containing n-3 Fatty Acid in Patients Considered After GI Surgery

A Prospective, Randomized, Double Blind Study to Compare the Efficacy and Safety of a n-3 Fatty Acid-containing Lipid Emulsion During Parenteral Nutrition in Patients Considered for Major Surgery for Gastric and Colorectal Cancer.

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
B. Braun Melsungen AG · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Evaluation of the impact of peri- and post-operative parenteral nutrition enriched with n-3 PUFA on post-operative inflammatory processes.

Conditions

Interventions

TypeNameDescription
DRUGMLF 54122-24 h i.v. infusion, maximum 0.75 ml lipid emulsion per kg BW per hour
DRUGLipofundin MCT22-24 h iv.infusion, maximum 0.75 ml lipid emulsion per kg BW per hour

Timeline

Start date
2008-11-01
Primary completion
2010-10-01
Completion
2010-10-01
First posted
2008-11-26
Last updated
2011-06-09

Locations

2 sites across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT00798447. Inclusion in this directory is not an endorsement.

Efficacy and Safety of a PN Regimen Containing n-3 Fatty Acid in Patients Considered After GI Surgery (NCT00798447) · Clinical Trials Directory