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Completed

NCT Number: NCT02468713

Effect on Blood Chemistry and Inflammatory Marker of Omega-3 Enriched Total Parenteral Nutrition

Fish oil is a rich source of omega-3 fatty acids, especially eicosapentanoic acid and docosahexaenoic acid, and it is not used widely in parenteral nutrition because fish oil emulsions have not been commercially available until very recently. The Objective of this study is to to evaluate the effect on blood lipid profiles of omega-3 enriched total parenteral nutrition in healthy Korean male subjects. This study is designed as a randomized, open-label, 2-treatment, 2-way crossover trial. Blood samples will be collected every 1 hour from 0 to 12 hours after starting an intravenous infusion for triglyceride, glucose, and insulin.

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Key information

Age range

30 year–55 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 4

Primary location

Chonbuk National University Hospital

Jeonju, Jeollabuk-do, 561712, South Korea

About this study

Fish oil is a rich source of omega-3 fatty acids, especially eicosapentanoic acid and docosahexaenoic acid, and it is not used widely in parenteral nutrition because fish oil emulsions have not been commercially available until very recently. The Objective of this study is to to evaluate the effect on blood lipid profiles of omega-3 enriched total parenteral nutrition in healthy Korean male subjects.

This study is designed as a randomized, open-label, 2-treatment, 2-way crossover trial. The 16 subjects will be randomly assigned to 1 of 2 sequences of the two treatments: Combiflex® lipid peri or Winuf® peri will be infused via peripheral venous catheter for 6 hours at 3 ml/kg/h. Blood samples will be collected every 1 hour from 0 to 12 hours after starting an intravenous infusion for triglyceride, glucose, and insulin. Cholesterol, HDL-cholesterol, LDL-cholesterol, AST, ALT, and total bilirubin as liver function biomarkers, and hsCRP as inflammatory biomarker will be analysed at 0, 6 and 12 hour after starting an intravenous infusion.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy male subjects between the ages of 30 and 55 years
  • Body Mass Index (BMI) of 17.5 to 30.5 kg/m2; and a total body weight >45 kg
  • An informed consent document signed and dated by the subject
  • Subjects who are willing and able to comply with all scheduled visits, treatment plan, laboratory tests, and other study procedures.

Exclusion criteria

  • Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease
  • Screening sitting blood pressure >150 mm Hg (systolic) or >90 mm Hg (diastolic)
  • Use of tobacco in excess of the equivalent of 20 cigarettes per day
  • Use of prescription or nonprescription drugs within 10 days
  • Blood donation within 2 months prior to dosing, or plasma donation within 1 month prior to dosing
  • Severe hyperlipidemic patients
  • Severe liver failure patients

Treatment and study plan

Combiflex® lipid peri

Drug

total parenteral nutrition solutions containing glucose, amino acids, electrolyte, soybean oil

Winuf® peri

Drug

total parenteral nutrition solution containing glucose, amino acids, electrolyte, soybean oil, medium chain triglyceride, olive oil and fish oil

Primary outcomes

  1. To compare AUC of plasma triglyceride between Winuf peri and Combiflex lipid peri

    Time frame: Before-dosing(0 hour) and 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, and 12 hours after dosing

    The wash-out period will be 7 days, and the second study period will be conducted on the same schedule as the first study period, with the exception of the assignment of the investigational product.

  2. To compare Cmax of plasma triglyceride between Winuf peri and Combiflex lipid peri

    Time frame: Before-dosing(0 hour) and 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, and 12 hours after dosing

    The wash-out period will be 7 days, and the second study period will be conducted on the same schedule as the first study period, with the exception of the assignment of the investigational product.

Secondary outcomes

  1. To compare AUC of plasma glucose between Winuf peri and Combiflex lipid peri

    Time frame: Before-dosing(0 hour) and 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, and 12 hours after dosing

  2. To compare Cmax of plasma glucose between Winuf peri and Combiflex lipid peri

    Time frame: Before-dosing(0 hour) and 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, and 12 hours after dosing

  3. To compare AUC of plasma insulin between Winuf peri and Combiflex lipid peri

    Time frame: Before-dosing(0 hour) and 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, and 12 hours after dosing

  4. To compare Cmax of plasma insulin between Winuf peri and Combiflex lipid peri

    Time frame: Before-dosing(0 hour) and 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, and 12 hours after dosing

  5. To compare AUC of plasma omega-3 between Winuf peri and Combiflex lipid peri

    Time frame: Before-dosing(0 hour) and 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, and 12 hours after dosing

  6. To compare Cmax of plasma omega-3 between Winuf peri and Combiflex lipid peri

    Time frame: Before-dosing(0 hour) and 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, and 12 hours after dosing

  7. Change from baseline in blood cholesterol level at 6 and 12 hours

    Time frame: Before-dosing(0 hour) and 6, and 12 hours

  8. Change from baseline in blood HDL-cholesterol level at 6 and 12 hours

    Time frame: Before-dosing(0 hour) and 6, and 12 hours

  9. Change from baseline in blood LDL-cholesterol level at 6 and 12 hours

    Time frame: Before-dosing(0 hour) and 6, and 12 hours

  10. Change from baseline in blood AST level at 6 and 12 hours

    Time frame: Before-dosing(0 hour) and 6, and 12 hours

  11. Change from baseline in blood ALT level at 6 and 12 hours

    Time frame: Before-dosing(0 hour) and 6, and 12 hours

  12. Change from baseline in blood total bilirubin level at 6 and 12 hours

    Time frame: Before-dosing(0 hour) and 6, and 12 hours

  13. Change from baseline in blood hsCRP level at 6 and 12 hours

    Time frame: Before-dosing(0 hour) and 6, and 12 hours

Sponsors and collaborators

Lead sponsor

Chonbuk National University Hospital

Other

Collaborators

  • JW Pharmaceutical

Registry information

Official study title

An Open Label, Randomized, Single Dose, Crossover Study to Evaluate the Effect on Blood Lipid Profiles of Omega-3 Enriched Total Parenteral Nutrition in Healthy Korean Male Subjects

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Jun 11, 2015
Registry last updated
Jun 11, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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