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Effect of Omega-3 Fatty Acids on the Perioperative Immune Response and Erythrocyte Function

Effect of Intravenous Omega-3 Fatty Acids on the Perioperative Immune Response and Erythrocyte Function in Patients With Colon Cancer

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02231203
Acronym
EMPIRE
Enrollment
44
Registered
2014-09-04
Start date
2014-10-31
Completion date
2016-06-30
Last updated
2018-07-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colon Cancer

Keywords

fish oil, omega-3 fatty acids, postoperative inflammatory response, erythrocyte function

Brief summary

Ideally, the postoperative inflammatory response is part of a well-orchestrated mechanism that contributes to tissue healing and rapid recovery. An exaggerated uncontrolled inflammatory response, however may lead to catabolism, tissue damage and organ failure. Omega-3 fatty acids may provide a means to alter cellular immune responses to the benefit of the patient. When omega-3 fatty acids are incorporated into membranes of inflammatory cells, they trigger intracellular signalling pathways that result in a less pro-inflammatory response. They modify gene and protein expression, modulate membrane protein activity and act as a reservoir for bioactive molecules. They also have a strong anti-inflammatory effect by mediating resolution of the inflammation. Furthermore, omega-3 fatty acids improve erythrocyte function, which is vital for an adequate microcirculation, tissue oxygenation and wound healing. The investigators hypothesize that the perioperative administration of intravenous omega-3 fatty acids results in a rapid incorporation in immune cells and erythrocytes, thereby reducing the postoperative inflammatory response and improving erythrocyte function in patients undergoing colorectal surgery.

Interventions

DRUGOmegaven

2 infusions, 2 ml/kg, one the night before operation and one the day after operation

DRUGPlacebo

2 infusions, 2 ml/kg, one the night before operation and one the day after operation

Sponsors

Medical Center Alkmaar
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients (male or female) undergoing elective laparoscopic surgery for colon cancer * Age between 60 and 80 years * BMI between 20 kg/m2 and below 30 kg/m2 * Written informed consent

Exclusion criteria

* Participation in or having participated in another clinical trial within the previous 3 months * Indications for continuously use of anticoagulant medication and no possibility to stop these medication perioperatively, for example patients with an artificial heart valve * Pre-operative Hemoglobin\<5.0 mmol/L * Metastatic disease * Very poor peripheral venous access * Current history of inflammatory or infectious disease * The use of anti-inflammatory drugs * The use of thyroid medication * The use of fish oil products or fish consumption more than 2 times a week * Contra-indication for the use of Omegaven-Fresenius, including: * General contra-indications for parenteral nutrition * Allergy to fish or egg protein.

Design outcomes

Primary

MeasureTime frameDescription
Change in ex vivo production of pro-inflammatory cytokine IL-6 in LPS stimulated whole bloodbaseline, day of surgery, postoperative day 1,2 and 4Ex vivo stimulation of whole blood with LPS (lipopolysaccharide, component of gram negative bacteria) resulting in the production of the pro-inflammatory cytokine IL-6, measured in ng/ml.

Secondary

MeasureTime frameDescription
Change in ex vivo production of TNF-α and IL-10 in LPS stimulated whole bloodbaseline, day of surgery, postoperative day 1, 2 and 4Ex vivo stimulation of whole blood with LPS (lipopolysaccharide, component of gram negative bacteria) resulting in the production of the pro-inflammatory cytokine TNF-α (tumor necrosis factor-α), and the anti-inflammatory cytokine IL-10 (interleukine-10), both measured in ng/ml.
Change in erythrocyte functionbaseline, day of surgery, postoperative day 1, 2 and 4Erythrocyte deformability and aggregation measured by LORRCA (laser assisted optical rotational red cell analyzer)
Change in in vivo systemic inflammatory response parametersbaseline, day of surgery, postoperative day 1, 2 and 4White blood cell count, C-reactive protein and cytokine levels (Interleukine-6, Tumor Necrosis Factor-α and Interleukine-10) in serum.

Other

MeasureTime frameDescription
Postoperative outcome (composite measure of length of stay and complications)Registration during admission, follow up 2 and 4 weeks after surgeryLength of hospital stay and occurence of surgical site infection, abscess, urinary tract infection, pneumonia, anastomotic leakage, need for Intensive Care Unit admission, Systemic Inflammatory Response Syndrome, Multi Organ Failure, any adverse events.
Cognitive functionbaseline, follow up 2 weeks after surgeryNeuropsychological examination using a reading test, an auditory verbal learning test, WAIS III figure series and trail making tests.

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026