Early Versus Delayed Enteral Feeding and Omega-3 Fatty Acid/Antioxidant Supplementation for Treating People With Acute Lung Injury or Acute Respiratory Distress Syndrome (The EDEN-Omega Study)

Respiratory Distress Syndrome, Adult Clinical Trial

— EDEN-Omega  

Official title:

Prospective, Randomized, Multi-Center Trial of Initial Trophic Enteral Feeding Followed by Advancement to Full-Calorie Enteral Feeding vs. Early Advancement to Full-Calorie Enteral Feeding in Patients With Acute Lung Injury (ALI) or Acute Respiratory Distress Syndrome (ARDS) and Prospective, Randomized, Blinded, Placebo-Controlled, Multi-Center Trial of Omega-3 Fatty Acid, Gamma-Linolenic Acid, and Anti-Oxidant Supplementation in the Management of Acute Lung Injury (ALI) or Acute Respiratory Distress Syndrome (ARDS)

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00609180
• Other study ID #: 549
• Secondary ID: N01-HR056179, HS
• Status: Terminated
• Phase: Phase 3
• First received: January 31, 2008
• Last updated: April 12, 2016
• Start date: December 2007
• Est. completion date: April 2009

Study information

• Verified date: February 2012
• Source: National Heart, Lung, and Blood Institute (NHLBI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

Acute respiratory distress syndrome (ARDS) and acute lung injury (ALI) are medical conditions that occur when there is severe inflammation and increased fluids in both lungs, making it difficult for the lungs to function properly. Hospital treatment for a person with ALI/ARDS often includes the use of a breathing machine, or ventilator, until the person is able to breathe without assistance. Initiating proper nutrition through a feeding tube early in a person's hospital stay may help to improve recovery, but the optimal timing, composition, and amount of feeding treatments are unknown. This study will evaluate whether early or delayed full-calorie feeding through a feeding tube is more effective in reducing recovery time and increasing survival rates in people with ALI/ARDS. The study will also determine whether supplementing the feedings with omega-3 fatty acids and antioxidants benefits people with ALI/ARDS.

Description:

ALI/ARDS involves extensive inflammation in the lungs that can lead to rapid respiratory failure. These conditions are most commonly caused by pneumonia, generalized infection, or severe trauma to the lungs, but can also be less commonly caused by smoke or salt water inhalation, drug overdose, or shock.

For some people, ALI/ARDS resolves without treatment, but many severe cases result in hospitalization in the intensive care unit (ICU), where 30% to 40% of cases end in mortality. Current treatments for ALI/ARDS include assisted breathing with a ventilator, supportive care, and management of the underlying causes. Enteral feeding, in which patients receive nutrition through a feeding tube, plays an important role in treatment, too. Some recent studies have shown that, compared to delayed feeding, enteral feeding initiated soon after a patient begins assisted breathing is associated with a shorter hospital stay and a better chance of survival. However, other studies show the opposite, and studies on optimal feeding volume and composition have conflicting results. Studies have also indicated that enhancing enteral feeding with omega-3 fatty acid and antioxidant supplements may help reduce lung inflammation, improving overall recovery rates. This study will evaluate the effects of early versus delayed full-calorie enteral feeding on mortality, ventilator-free days, ICU-free days, and organ failure in people with ALI/ARDS. The study will also determine whether supplementation with omega-3 fatty acid and antioxidants adds any beneficial effect.

Upon admission to the ICU, a dietary evaluation will be done on each participant to determine goal, or full-calorie, feeding rates, which will be based on body weight and daily energy consumption. Participants will also undergo baseline assessments and procedures, which will include vital sign measurements, blood draws, a frontal chest radiograph, ventilator settings, and placement of feeding tube. Participants will be randomly assigned to receive initial enteral feedings that are either minimal (trophic) or full-calorie. They will also be randomly assigned to receive either omega-3 fatty acid and antioxidant supplementation or placebo. All participants will begin enteral feeding within 6 hours of treatment assignment.

Participants assigned to initial minimal enteral feedings will receive feedings at 10 cubic centimeters (cc) per hour, to be continued at this rate for 144 hours, provided that the participant remains on the ventilator. After the 144 hours, the feeding rate will be advanced to full-calorie rates.

Participants assigned to initial full-calorie enteral feedings will receive feedings at 25 cc per hour, and the feeding rate will be increased by 25 cc per hour every 6 hours until goal rate is reached. During enteral feedings, gastric residual volumes (GRVs) will be checked every 6 to 12 hours to assure acceptable levels. Participants will complete enteral feedings upon hospital discharge, Day 28 of treatment, death, or ability to achieve 48 hours of unassisted breathing. Omega-3 fatty acid, antioxidant, and placebo supplements will be administered with a syringe into the participant's feeding tube every 12 hours until Day 21 or discontinuation of the ventilator.

Blood pressure, heart rate, ventilation settings, and various blood factors will be measured during treatment. Phone-based follow-up assessments will occur at Months 6 and 12 after ICU discharge and will include measurements of health-related quality of life; psychological, neurocognitive, and physical activity outcomes; healthcare utilization; and mortality.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 272
• Est. completion date: April 2009
• Est. primary completion date: February 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 13 Years and older

Eligibility

Inclusion Criteria:

• Must meet the following three criteria at study entry within a 24-hour period: 1) PaO2/FiO2 less than or equal to 300 (if altitude is more than 1000 meters, then PaO2/FiO2 less than or equal to 300 x [barometric pressure/760]), 2) bilateral infiltrates (patchy, diffuse, homogeneous, or asymmetric) consistent with pulmonary edema on frontal chest radiograph, and 3) requirement for positive pressure ventilation via endotracheal tube

• No clinical evidence of left-sided cardiac failure to account for bilateral pulmonary infiltrates

• Intention of primary medical team to enterally feed the patient

• Undergoes enteral feeding within 48 hours of meeting inclusion criteria

Exclusion Criteria:

• Neuromuscular disease that impairs ability to breath without assistance, such as cervical spinal cord injury at level C5 or higher, amyotrophic lateral sclerosis, Guillain-Barré syndrome, or myasthenia gravis

• Pregnant or breastfeeding

• Severe chronic respiratory disease. More information about this criterion can be found in the protocol.

• Burns on greater than 40% total body surface area

• Malignancy or other irreversible disease or condition for which 6-month mortality is estimated to be greater than 50%. More information about this criterion can be found in the protocol.

• Allogeneic bone marrow transplant within the 5 years before study entry

• Patient, surrogate, or physician not committed to full support (exception: a patient will not be excluded if he/she would receive all supportive care except for attempts at resuscitation from cardiac arrest)

• Severe chronic liver disease (Child-Pugh score of 11 to 15)

• Diffuse alveolar hemorrhage from vasculitis

• Morbid obesity, defined as 1 kg/cm body weight

• Unwilling or unable to use the ARDS network 6 mL/kg PBW ventilation protocol

• Moribund patient not expected to survive 24 hours

• No intent to obtain central venous access for monitoring intravascular pressures

• More than 72 hours since mechanical ventilation initiated

• Refractory shock. More information about this criterion can be found in the protocol.

• Unable to obtain enteral access

• Presence of partial or complete mechanical bowel obstruction

• Presence of ischemia or infarction

• Current total parenteral nutrition (TPN) use or intent to use TPN within 7 days of study entry

• Severe malnutrition with body mass index less than 18.5 or loss of more than 30% total body weight in the 6 months before study entry

• Laparotomy expected within 7 days of study entry

• Unable to raise head of bed 30 to 45 degrees

• Short-bowel syndrome or absence of gastrointestinal tract

• Presence of high-output (greater than 500 cc/day) enterocutaneous fistula

• International normalized ratio greater than 5.0, platelet count less than 30,000/mm3, or history of bleeding disorder

• Intracranial hemorrhage within the 1 month before study entry

• Allergy to enteral formula, omega-3 fatty acids, GLA, vitamin E, vitamin C, beta-carotene, taurine, or L-carnitine

• Requirement for, or physician insistence on, enteral formula supplemented with omega-3 fatty acids (ex: Oxepa®, Impact®) or providing omega-3 fatty acid, GLA, or antioxidant supplementation

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Acute Lung Injury
• Lung Injury
• Respiratory Distress Syndrome, Adult
• Respiratory Distress Syndrome, Newborn
• Syndrome

Intervention

Behavioral:
• Minimal (Trophic) Feeding
Enteral feeds will be started at 10 cc per hour and continued at this rate for 144 hours. After 144 hours of trophic enteral feeds, the feeding rate will be advanced to full-calorie rates, which will continue for the duration of mechanical ventilation up to Day 28.
• Full Feeding
Upon admission to the ICU, a full-calorie feeding rate will be determined, which will be calculated to deliver 25 to 35 kcal/kg predicted body weight (PBW) each day. Enteral feeds will be initiated at 25 cc per hour. The feeding rate will be increased by 25 cc per hour every 6 hours until goal rate is achieved, which will be administered for the duration of mechanical ventilation up to Day 28.

Dietary Supplement:
• Omega-3 Fatty Acids and Antioxidant Supplements
Omega-3 fatty acids, GLA, and antioxidants will be administered through a feeding tube every 12 hours as a 120-cc bolus. Dosing will continue for 21 days or until discontinuation of mechanical ventilation.
• Placebo
The study placebo will be administered through a feeding tube every 12 hours as a 120 cc bolus. Dosing will continue for 21 days or until discontinuation of mechanical ventilation.

Locations

Country	Name	City	State
United States	Baltimore VA Medical Center	Baltimore	Maryland
United States	Johns Hopkins Bayview Medical Center	Baltimore	Maryland
United States	Johns Hopkins Hospital	Baltimore	Maryland
United States	University of Maryland Shock Trauma Center	Baltimore	Maryland
United States	Baton Rouge General Hospital-Blue Bonnet	Baton Rouge	Louisiana
United States	Baton Rouge General Hospital-Midcity	Baton Rouge	Louisiana
United States	Earl K. Long Medical Center	Baton Rouge	Louisiana
United States	Our Lady of the Lake Regional Medical Center	Baton Rouge	Louisiana
United States	University of North Carolina	Chapel Hill	North Carolina
United States	University of Virginia Medical Center	Charlottesville	Virginia
United States	Cleveland Clinic Foundation	Cleveland	Ohio
United States	MetroHealth Medical Center	Cleveland	Ohio
United States	University Hospitals of Cleveland	Cleveland	Ohio
United States	Centura St. Anthony Central Hospital	Denver	Colorado
United States	Denver Health Medical Center	Denver	Colorado
United States	Rose Medical Center	Denver	Colorado
United States	University of Colorado Health Sciences Center	Denver	Colorado
United States	Duke University Medical Center	Durham	North Carolina
United States	Durham Regional Medical Center	Durham	North Carolina
United States	University of San Francisco-Fresno Medical Center	Fresno	California
United States	Moses Cone Health System	Greensboro	North Carolina
United States	Wesley Long Community Hospital	Greensboro	North Carolina
United States	Baylor College of Medicine	Houston	Texas
United States	Intermountain Medical Center	Murray	Utah
United States	Vanderbilt University Medical Center	Nashville	Tennessee
United States	Medical Center of Louisiana	New Orleans	Louisiana
United States	Ochsner Clinic Foundation	New Orleans	Louisiana
United States	Tulane University Health Sciences Center	New Orleans	Louisiana
United States	McKay-Dee Hospital	Ogden	Utah
United States	Utah Valley Regional Medical Center	Provo	Utah
United States	Rochester Methodist Hospital	Rochester	Minnesota
United States	St. Mary's Hospital, Mayo Clinic	Rochester	Minnesota
United States	University of California, Davis Medical Center	Sacramento	California
United States	LDS Hospital	Salt Lake City	Utah
United States	UCSF-Moffitt Hospital	San Francisco	California
United States	UCSF-San Francisco General Hospital	San Francisco	California
United States	Harborview Medical Center	Seattle	Washington
United States	University of Washington	Seattle	Washington
United States	Baystate Medical Center	Springfield	Massachusetts
United States	Washington Hospital Center	Washington DC	District of Columbia
United States	Wake Forest University Baptist Medical Center	Winston Salem	North Carolina

Sponsors (1)

Lead Sponsor	Collaborator
National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of ventilator-free days (VFD)		Measured at Day 28	No
Primary	Mortality before hospital discharge, with unassisted breathing		Measured at Days 60 and 90	Yes
Secondary	Number of intensive care unit-free days		Measured at Day 28	No
Secondary	Number of organ failure-free days (liver, kidney, heart, central nervous system, and hematologic)		Measured at Day 28	No
Secondary	Incidence of ventilator-associated pneumonia		Measured at Day 28	No
Secondary	Number of days from first meeting criteria for weaning readiness to Day 28		Measured at Day 28	No
Secondary	VFDs and mortality in participants with a partial pressure of oxygen in arterial blood (PaO2)/fraction of inspired oxygen (FIO2) less than or equal to 200 or with shock at the time of study entry		Measured at Days 28 and 60, respectively	Yes
Secondary	Change in plasma and mini-bronchoalveolar lavage (BAL) levels of interleukin (IL)-6, IL-8, von Willebrand factor (VWF), surfactant protein D (SPD), and total protein concentrations		Measured at Day 3	No
Secondary	Health-related quality of life; healthcare utilization; and psychological, neurocognitive, and physical activity outcomes		Measured at Months 6 and 12	No
Secondary	Duration of survival after hospital discharge using the National Death Index		Measured at Months 6 and 12	Yes

External Links

•   Click Here for the NHLBI Acute Respiratory Distress Syndrome Network Website