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A Phase II Randomized Trial of Fish Oil in Patients With Acute Lung Injury (ALI)
This study is currently recruiting participants.
Verified by University of Washington, October 2008
Sponsors and Collaborators: University of Washington
National Heart, Lung, and Blood Institute (NHLBI)
American Thoracic Society
Acute Respiratory Distress Syndrome Foundation
American Society for Parenteral and Enteral Nutrition
Information provided by: University of Washington
ClinicalTrials.gov Identifier: NCT00351533
  Purpose

The purpose of this study is to determine whether fish oil (containing omega-3 fatty acids) given enterally is safe and effective in reducing lung and systemic inflammation seen in acute lung injury.


Condition Intervention Phase
Respiratory Distress Syndrome, Adult
Acute Lung Injury
Acute Respiratory Distress Syndrome
Drug: Fish oil (eicosapentaenoic acid and docosahexanoic acid)
Phase II

Drug Information available for: Fish oil Docosahexaenoic acids Eicosapentaenoic acid
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment
Official Title: A Randomized, Double-Blind Study of the Effect of Fish Oil (Eicosapentaenoic Acid and Docosahexanoic Acid) on Lung and Systemic Inflammation in Patients With Acute Lung Injury (ALI)

Further study details as provided by University of Washington:

Primary Outcome Measures:
  • Bronchoalveolar lavage fluid interleukin-8 [ Time Frame: Days 5 and 9 ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • BALF leukotriene B4, interleukin-6, interleukin-1β, interleukin-1 receptor antagonist, tumor necrosis factor α, neutrophil count, procollagen peptide III, macrophage inhibitory peptide-1-α, vonWillebrand factor [ Time Frame: Days 5 and 9 ] [ Designated as safety issue: No ]
  • Lung compliance and oxygenation [ Time Frame: Throughout ICU stay ] [ Designated as safety issue: No ]
  • Serum interleukin-8, leukotriene B4, interleukin-6, interleukin-1β [ Time Frame: Days 5 and 9 ] [ Designated as safety issue: No ]
  • Organ failure (quantified by SOFA scores), ventilator-free days during first 28 days, ICU length of stay, hospital length of stay, nosocomial infections, hospital mortality [ Time Frame: Throughout hospital stay ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 90
Study Start Date: July 2006
Estimated Study Completion Date: March 2009
Estimated Primary Completion Date: December 2008 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental
Enteral fish oil
Drug: Fish oil (eicosapentaenoic acid and docosahexanoic acid)
Liquid fish oil 7.5cc enterally every 6 hours
2: Placebo Comparator
Saline
Drug: Fish oil (eicosapentaenoic acid and docosahexanoic acid)
Liquid fish oil 7.5cc enterally every 6 hours

Detailed Description:

Acute lung injury (ALI) is common among critically ill patients and is associated with a high case fatality. Only one intervention has been shown to improve survival in a large clinical trial, and new therapies targeting the inflammatory response are needed. Nutrient interventions may provide benefit; specifically there is plausible biologic rationale for administering n-3 fatty acids (n-3 FAs) found in fish oil to patients with ALI, as n-3 FAs decrease formation of eicosanoid inflammatory mediators. However, although promising results have emerged from prior studies, fish oils have only been tested in ALI patients in a commercial enteral formula containing additional nutrients, and the control group received a high-fat enteral formula that may have been proinflammatory. Therefore, no conclusion can be drawn about the independent effect of fish oils. Furthermore, the inclusion of key pharmaconutrients in feeding formulas, instead of delivering them separately as pharmaceuticals, limits exposure to the agent, as ICU patients commonly receive less than 60% of prescribed caloric needs. Finally, specialized feeding formulas are very expensive, and it may be substantially cheaper to administer pharmaconutrients separately. We believe it is time to begin to approach nutrient trials in critically ill patients differently -- to move away from including them in feeding formulas and begin delivering them like pharmaceuticals. With appropriate scientific investigation and the use of non-nutrient placebos, this novel and innovative approach is a new paradigm of investigating nutrient delivery to critically ill patients.

This study is a phase II randomized controlled trial to determine the effects of enteral eicosapentaenoic acid (EPA) and docosahexanoic acid (DHA), both n-3 FAs found in fish oil, versus placebo on the pulmonary and systemic environments, and on clinical outcomes, in patients with ALI. We will investigate the effect of fish oil administration on several biological markers of injury and inflammation in bronchoalveolar lavage fluid and serum, on pulmonary physiologic outcomes, and on clinical outcomes.

Comparison(s): Mechanically ventilated patients with acute lung injury randomized to receive enteral fish oil versus compared to mechanically ventilated patients with acute lung injury randomized to receive placebo.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Requiring positive-pressure mechanical ventilation
  • ALI criteria: PaO2/FiO2 <300, bilateral infiltrates on CXR, no left atrial hypertension
  • Age > 17 years

Exclusion Criteria:

  • Expected ICU length of stay <48 hours
  • Unable to undergo BAL at enrollment
  • Unable to obtain enteral access
  • Post-cardiac arrest with suspected significant anoxic brain injury
  • Expected survival < 28 days
  • Pregnant
  • Platelet count < 30,000, active bleeding, or INR>3.0
  • History of ventricular tachycardia or fibrillation
  • Receiving rh-APC for sepsis
  • AIDS with CD4 count < 200
  • Metastatic cancer
  • History of bone marrow, lung, liver, cardiac, kidney, or pancreas transplant
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00351533

Contacts
Contact: Renee D. Stapleton, MD, MSc 206-849-4843 rstaplet@u.washington.edu
Contact: Stephanie Gundel, RD 206-341-4041 sgundel@u.washington.edu

Locations
United States, Idaho
St. Alphonsus Medical Center Recruiting
Boise, Idaho, United States, 83706
Contact: Joseph Crowley, MD     208-855-1002     josecrow@cableone.net    
Principal Investigator: Joseph Crowley, MD            
United States, Oregon
Oregon Health Sciences University Completed
Portland, Oregon, United States, 97239
United States, Vermont
University of Vermont/Fletcher Allen Health Care Recruiting
Burlington, Vermont, United States, 05401
Contact: Renee D. Stapleton, MD, MSc     206-849-4843     renee.stapleton@uvm.edu    
Principal Investigator: Renee D. Stapleton, MD, MSc            
United States, Washington
Harborview Medical Center Recruiting
Seattle, Washington, United States, 98104
Contact: Stephanie Gundel, RD     206-341-4041     sgundel@u.washington.edu    
Principal Investigator: Margaret J. Neff, MD, MSc            
Sub-Investigator: Renee D. Stapleton, MD MSc            
Canada, Ontario
St. Michael's Hospital Completed
Toronto, Ontario, Canada, M5B1W8
Sponsors and Collaborators
University of Washington
American Thoracic Society
Acute Respiratory Distress Syndrome Foundation
American Society for Parenteral and Enteral Nutrition
Investigators
Principal Investigator: Renee D. Stapleton, MD, MSc University of Vermont
  More Information

Responsible Party: University of Washington ( Renee D. Stapleton )
Study ID Numbers: 05-7895-A 03
Study First Received: July 11, 2006
Last Updated: October 8, 2008
ClinicalTrials.gov Identifier: NCT00351533  
Health Authority: United States: Institutional Review Board

Keywords provided by University of Washington:
Respiratory distress syndrome, adult
Acute lung injury
Acute respiratory distress syndrome
ARDS, human
Fish oils
Fatty Acids, Omega-3
Docosahexaenoic Acids
Eicosapentaenoic Acid

Study placed in the following topic categories:
Respiratory Tract Diseases
Lung Diseases
Respiration Disorders
Respiratory Distress Syndrome, Adult
Acute respiratory distress syndrome
Inflammation

Additional relevant MeSH terms:
Pathologic Processes
Disease
Syndrome

ClinicalTrials.gov processed this record on January 14, 2009