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OpenTrials
Completed

NCT Number: NCT00798447

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

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

Completed

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Kaohsiung Medical University Hospital, Kaohsiung City, Taiwan

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Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients considered for major surgery for gastric and colorectal cancer
  • expected requirement for post operative PN or TPN of at least 7 days
  • possibility of PN/TPN provision 1 day prior to surgery
  • Age >18 years old and <80 years old
  • Hemodynamically stable
  • Written Informed consent

Exclusion criteria

  • Participation in a clinical study with an investigational drug or an investigational medical device within one month prior to the start of study
  • Patients with sepsis, severe sepsis or septic shock
  • Known or suspected drug abuse
  • Intrahepatic cholestasis
  • General contraindications for infusion therapy such as acute pulmonary edema, hyperhydration and decompensated cardiac insufficiency
  • Pregnancy (positive in urine) or lactation
  • Autoimmune disease e.g. HIV
  • Known hypersensitivity to egg-, soy-, and fish proteins or any of the ingredients of the investigational products
  • Hemodynamic failure of any origin (hemorrhagic shock, myocardial infarction, cardiac failure)
  • Alterations of coagulation (thrombocytes <150000 /mm3), PT < 50%, PTT > 40 sec
  • Ketoacidosis caused by Diabetes mellitus within 7 days prior to onset of study
  • Renal insufficiency with serum creatinine > 1.4 mg/dL (>124 µmol/L)
  • Patients with severe liver dysfunction with bilirubin >2.5 mg/dL (> 43 µmol/L)
  • Lipid disorders, in particular fasting serum triglycerides > 250 mg/dL (>2.85 mmol/L),

Treatment and study plan

MLF 541

Drug

22-24 h i.v. infusion, maximum 0.75 ml lipid emulsion per kg BW per hour

Lipofundin MCT

Drug

22-24 h iv.infusion, maximum 0.75 ml lipid emulsion per kg BW per hour

Primary outcomes

  1. reduction of pro inflammatory activity

    Time frame: 30 days

Sponsors and collaborators

Lead sponsor

B. Braun Melsungen AG

Industry

Collaborators

  • B.Braun Taiwan Co., Ltd.

Registry information

Official study title

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.

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Nov 26, 2008
Registry last updated
Jun 9, 2011

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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