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UnknownNCT01819961

Parenteral Fish Oil in Major Laparoscopic Abdominal Surgery

Randomized Clinical Trial of Omega-3 Fatty Acid-supplemented Parenteral Nutrition Versus Standard Parenteral Nutrition in Patients Undergoing Major Laparoscopic Abdominal Surgery

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Wei Zhou · Academic / Other
Sex
All
Age
15 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to assess the effect of postoperative parenteral fish oil on clinical outcome and immune function after major laparoscopic abdominal surgery.

Detailed description

Postoperative patients are randomized by a sealed envelope to receive either a 50:50 (vol/vol) mixture of an oil rich in medium-chain fatty acids and soybean oil (termed MCT/LCT) or a mixture of MCT/LCT and fish oil Omegaven for 7 days. Full blood count, biochemistry and coagulation are routinely assessed. Fresh blood samples are centrifuged into plasma, red blood cells and lymphocytes then stored at -80°C pending analysis. The primary endpoint was numbers of infective complications.Secondary endpoints were other clinical outcomes, length of hospital stay, and in-hospital mortality, along with plasma immunological markers.

Conditions

Interventions

TypeNameDescription
DRUGMCT/LCT and fish oil
DRUGMCT/LCT

Timeline

Start date
2013-04-01
Primary completion
2013-10-01
Completion
2013-12-01
First posted
2013-03-28
Last updated
2013-03-28

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT01819961. Inclusion in this directory is not an endorsement.