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Impact of Omega-3 Fatty Acids on Lactate

E

Ege University

Status

Completed

Conditions

Gastric Surgery

Treatments

Drug: Lipovenoes® 10% and Omegaven®,

Study type

Interventional

Funder types

Other

Identifiers

NCT00929461
B.30.2.EGE.0.01.00.00/7EM/458

Details and patient eligibility

About

Pre- and intra-operative nutritional support in patient undergoing major surgery results in decreased morbidity and mortality. Studies investigating the role of omega-3 fatty acids in these patients are increasing. Some are focused on perfusion at the cellular level. This study was undertaken to address the effect of postoperative administration of omega-3 fatty acids on cellular hypoperfusion associated with major gastric surgery.

Sex

All

Ages

25 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing major gastric cancer surgery

Exclusion criteria

  • None

Trial design

0 participants in 2 patient groups

Omega-3 group
Other group
Description:
All patients received TPN for 5 days postoperatively, according to a standard protocol: 3 g/kg BW glucose (5% Dextrose in Ringer's Lactate, Biosel, Istanbul), 1.2 g/kg BW amino acids (Aminosteril 10%, Fresenius-Kabi) and 0.8 g/kg BW omega-6 fatty acids (Lipovenoes® 10%, Fresenius-Kabi) were provided to both groups through an indwelling central venous catheter. In the omega-3 group, the lipid content of TPN was replaced partially by omega-3 fatty acids (Omegaven®, Fresenius-Kabi) up to 0.2 g/kg BW per day.
Treatment:
Drug: Lipovenoes® 10% and Omegaven®,
Omega 3 + Omega 6 group
Other group
Description:
All patients received TPN for 5 days postoperatively, according to a standard protocol: 3 g/kg BW glucose (5% Dextrose in Ringer's Lactate, Biosel, Istanbul), 1.2 g/kg BW amino acids (Aminosteril 10%, Fresenius-Kabi) and 0.8 g/kg BW omega-6 fatty acids (Lipovenoes® 10%, Fresenius-Kabi) were provided to both groups through an indwelling central venous catheter.
Treatment:
Drug: Lipovenoes® 10% and Omegaven®,

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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