search
Back to results

The Chronic Obstructive Pulmonary Disease Fish Oil Pilot Trial (COD-Fish)

Primary Purpose

Chronic Obstructive Pulmonary Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
n-3 polyunsaturated fatty acids
Placebo
Sponsored by
Columbia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease focused on measuring Clinical Trials, Randomized

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Post-bronchodilator FEV1/FVC ratio <70%
  • Post-bronchodilator FEV1 <65% predicted.
  • Clinical diagnosis of COPD
  • Stable medical regimen for 30 days prior to enrollment
  • Age > 40 years old
  • History of former cigarette smoking, > or = 10 pack years

Exclusion Criteria:

  • COPD exacerbation or hospitalization for COPD in the past 30 days
  • Confirmed history of physician-diagnosed asthma
  • History of unrelated pulmonary disease (e.g. interstitial lung disease, thromboembolic disease)
  • Status-post lung transplantation or Lung volume reduction surgery (LVRS)
  • Systolic blood pressure >170mmHg or<100mmHg at rest, diastolic blood pressure >100 at rest, or resting HR >120.
  • Active cigarette smoking
  • Clinical diagnosis of left-sided congestive heart failure
  • Clinical diagnosis of coronary artery disease
  • Clinical diagnosis of cerebrovascular disease
  • Clinical diagnosis of peripheral vascular disease
  • Prior history of stroke or myocardial infarction
  • Clinical diagnosis of obstructive sleep apnea
  • Pregnancy (known, and screen with urine BHCG) or current breastfeeding
  • Contraindication to Omax3[TM] use, including a history of hypersensitivity to Omax3[TM]
  • Current use of high-dose fish oil capsules (defined as >1 or 2 grams/day of omega-3 fatty acids)
  • Current use of Coumadin
  • Elevated ALT greater than 2 times the upper limit of normal at baseline
  • Congenital abnormality of the arm or hand
  • Raynaud's Phenomenon
  • History of radical mastectomy or removal or axillary lymph nodes
  • Allergy to fish or corn oil
  • Unstable angina during previous month
  • End Stage Liver Disease, Cirrhosis

For Non-COPD controls (Same Inclusion and exclusion criteria, except for inclusion, must NOT have the following:)

  • Post-bronchodilator FEV1/FVC ratio >70%
  • Post-bronchodilator FEV1 <65% predicted.
  • Clinical diagnosis of COPD

Sites / Locations

  • Columbia University Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo (corn oil)

PUFA (Omax3)

Arm Description

Each participant will be taking 3 capsules of a matching placebo (corn oil).

Omax3[TM] (Cenestra Health), or dietary supplement: n-3 polyunsaturated fatty acids, is a 1 gram softgel capsule containing 94.5% omega-3 fatty acids. Each participant will be taking 3 capsules of Omax3[TM].

Outcomes

Primary Outcome Measures

Percent Flow Mediated Dilation (FMD)

Secondary Outcome Measures

Serum level of LTB4
Serum level of TNF-alpha
Serum level of IFN-gamma
Difference in Pre- and Post-bronchodilator Spirometry
Average six-minute-walk test distance
Average St. George's Respiratory Questionnaire score
Change in percent of Peripheral Arterial Tonometry (EndoPAT)
Number of endothelial cell protein expression

Full Information

First Posted
October 22, 2008
Last Updated
November 16, 2020
Sponsor
Columbia University
Collaborators
National Institute of Environmental Health Sciences (NIEHS)
search

1. Study Identification

Unique Protocol Identification Number
NCT00835289
Brief Title
The Chronic Obstructive Pulmonary Disease Fish Oil Pilot Trial
Acronym
COD-Fish
Official Title
The Chronic Obstructive Pulmonary Disease Fish Oil Pilot Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Completed
Study Start Date
March 2009 (undefined)
Primary Completion Date
August 2013 (Actual)
Study Completion Date
August 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Columbia University
Collaborators
National Institute of Environmental Health Sciences (NIEHS)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Chronic obstructive pulmonary disease (COPD) is currently the fourth leading cause of death in the United States. Unlike the other leading causes of death, no medical therapies currently available improve the course of disease or affect survival in COPD. Recent investigations suggest that endothelial dysfunction and chronic inflammation is fundamental to COPD. Fish oil intake improves endothelial dysfunction and lowers levels of inflammatory intermediaries which may be important in the development of COPD. The Chronic Obstructive Pulmonary Disease Fish Oil (COD-Fish) Pilot Trial will enroll 40-45 participants with COPD. These participants will be randomized to receive omega-3 polyunsaturated fatty acid supplementation (PUFA) or placebo (containing corn oil). All participants will perform a number of noninvasive tests (including flow-mediated dilation (FMD) and pulmonary function testing) at study entry as well as every two months for a total of six months. Thirty participants who agree to it will undergo a separate procedure to collect cells from inside a forearm vein for analysis to be compared to 30 controls. The main purpose of this trial is to examine the effect of PUFA on endothelial function as measured by change in FMD in patients with COPD. We hypothesize that in subjects with COPD, treatment with PUFA will increase FMD.
Detailed Description
Chronic obstructive pulmonary disease is abbreviated as COPD and includes both emphysema and chronic bronchitis. COPD is currently the fourth leading cause of death in the United States. Unlike most major medical diseases, the morbidity and mortality from COPD continue to rise in the US. In 2000, over 10 million Americans carried a physician diagnosis of COPD and 120,000 Americans died from this disease. Additionally, from the year 1980 to the year 2000, the number of cases of COPD among women nearly doubled and the prevalence among African Americans increased by 61%. Unlike the other leading causes of death, no medical therapies currently available improve the course of disease or affect survival in COPD. Current therapies for COPD that improve survival in COPD are limited to smoking cessation, oxygen therapy, and possibly surgery. Medical therapies such as inhalers and pills improve symptoms and reduce COPD exacerbations ("attacks"), but have not been shown to slow down the progression of the disease. Recent investigations suggest that endothelial dysfunction and chronic inflammation is fundamental to COPD. Fish oil intake improves endothelial dysfunction and lowers levels of inflammatory intermediaries. These inflammatory intermediaries can be measured in the blood and are potentially important in the development of COPD. Large observational studies demonstrate that participants who eat high amounts of fish oil develop less COPD and have lower levels of these inflammatory intermediaries. The Chronic Obstructive Pulmonary Disease Fish Oil (COD-Fish) Pilot Trial will enroll 40-45 participants with COPD. These participants will be randomized to receive Omax3[TM] or placebo (containing corn oil). Omax3[TM] (Cenestra Health) is a 1 gram softgel capsule containing 94.5% omega-3 fatty acids. Each participant will be taking 3 capsules of either Omax3[TM] or matching placebo. The investigators and the subjects will be blinded, meaning that neither the investigators nor the subjects will know if they are taking Omax3[TM] or placebo. All participants will perform a number of noninvasive tests at study entry as well as every two months for a total of six months. They will also undergo pulmonary function testing, flow-mediated dilation (FMD), peripheral arterial tonometry (PAT), six minute-walk tests (6MWT), blood drawing and answer questionnaire data. Thirty participants who agree to it will undergo a separate procedure to collect cells from inside a forearm vein for analysis to be compared to 30 controls. The main purpose of this trial is to examine the effect of Omax3[TM] on endothelial function as measured by change in FMD in patients with COPD. We hypothesize that in subjects with COPD, treatment with Omax3[TM] will increase FMD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease
Keywords
Clinical Trials, Randomized

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo (corn oil)
Arm Type
Placebo Comparator
Arm Description
Each participant will be taking 3 capsules of a matching placebo (corn oil).
Arm Title
PUFA (Omax3)
Arm Type
Experimental
Arm Description
Omax3[TM] (Cenestra Health), or dietary supplement: n-3 polyunsaturated fatty acids, is a 1 gram softgel capsule containing 94.5% omega-3 fatty acids. Each participant will be taking 3 capsules of Omax3[TM].
Intervention Type
Dietary Supplement
Intervention Name(s)
n-3 polyunsaturated fatty acids
Other Intervention Name(s)
Omax-3, PUFA, Omega-3
Intervention Description
Omax3[TM] (Cenestra Health [TM]) is a 1 g softgel capsule containing 94.5% omega-3 fatty acids. Each serving size is a 1 gram capsule, which contains 690 mg of eicosapentanoic acid (EPA) and 182 mg of docosahexanoic acid (DHA). Inactive ingredients include: Vitamin E/Tocopherol 2294 ppm (in a carrier of partially hydrogenated vegetable oils including soybean oil), gelatin, glycerol, and purified water (components of the capsule shell). The study participants will be randomized to 3 softgel capsules a day for 6 months.
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
3 capsules of matching corn oil placebo
Primary Outcome Measure Information:
Title
Percent Flow Mediated Dilation (FMD)
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Serum level of LTB4
Time Frame
6 months
Title
Serum level of TNF-alpha
Time Frame
6 months
Title
Serum level of IFN-gamma
Time Frame
6 months
Title
Difference in Pre- and Post-bronchodilator Spirometry
Time Frame
6 months
Title
Average six-minute-walk test distance
Time Frame
6 months
Title
Average St. George's Respiratory Questionnaire score
Time Frame
6 months
Title
Change in percent of Peripheral Arterial Tonometry (EndoPAT)
Time Frame
4 months
Title
Number of endothelial cell protein expression
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Post-bronchodilator FEV1/FVC ratio <70% Post-bronchodilator FEV1 <65% predicted. Clinical diagnosis of COPD Stable medical regimen for 30 days prior to enrollment Age > 40 years old History of former cigarette smoking, > or = 10 pack years Exclusion Criteria: COPD exacerbation or hospitalization for COPD in the past 30 days Confirmed history of physician-diagnosed asthma History of unrelated pulmonary disease (e.g. interstitial lung disease, thromboembolic disease) Status-post lung transplantation or Lung volume reduction surgery (LVRS) Systolic blood pressure >170mmHg or<100mmHg at rest, diastolic blood pressure >100 at rest, or resting HR >120. Active cigarette smoking Clinical diagnosis of left-sided congestive heart failure Clinical diagnosis of coronary artery disease Clinical diagnosis of cerebrovascular disease Clinical diagnosis of peripheral vascular disease Prior history of stroke or myocardial infarction Clinical diagnosis of obstructive sleep apnea Pregnancy (known, and screen with urine BHCG) or current breastfeeding Contraindication to Omax3[TM] use, including a history of hypersensitivity to Omax3[TM] Current use of high-dose fish oil capsules (defined as >1 or 2 grams/day of omega-3 fatty acids) Current use of Coumadin Elevated ALT greater than 2 times the upper limit of normal at baseline Congenital abnormality of the arm or hand Raynaud's Phenomenon History of radical mastectomy or removal or axillary lymph nodes Allergy to fish or corn oil Unstable angina during previous month End Stage Liver Disease, Cirrhosis For Non-COPD controls (Same Inclusion and exclusion criteria, except for inclusion, must NOT have the following:) Post-bronchodilator FEV1/FVC ratio >70% Post-bronchodilator FEV1 <65% predicted. Clinical diagnosis of COPD
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
R Graham Barr, MD/DrPH
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Columbia University Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
33150779
Citation
Kim JS, Thomashow MA, Yip NH, Burkart KM, Lo Cascio CM, Shimbo D, Barr RG. Randomization to Omega-3 Fatty Acid Supplementation and Endothelial Function in COPD: The COD-Fish Randomized Controlled Trial. Chronic Obstr Pulm Dis. 2021 Jan;8(1):41-53. doi: 10.15326/jcopdf.8.1.2020.0132.
Results Reference
result

Learn more about this trial

The Chronic Obstructive Pulmonary Disease Fish Oil Pilot Trial

We'll reach out to this number within 24 hrs