A Fish Oil Supplement to Maintain Body Weight in Patients With Disease-Related Weight Loss

Johns Hopkins Medicine

Status and phase

Completed

Phase 2

Conditions

Chronic Heart Failure

Chronic Obstructive Pulmonary Disease

Cancer

Cancer Cachexia

Rheumatoid Arthritis

Treatments

Drug: Fish oil supplement

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT00094562

P50AT000437 (U.S. NIH Grant/Contract)

J0275

03-02-10-12 (Other Identifier)

Details and patient eligibility

About

The purpose of this study is to evaluate the safety and effectiveness of fish oil supplements in maintaining weight in people with disease-related weight loss and/or cachexia.

Full description

The overall goal of this project is to evaluate the safety and efficacy of nutritional supplementation with fish oils to maintain weight in patients with disease-related weight loss (cachexia). Weight loss commonly results in a poorer prognosis, functional status, and quality of life. Despite the high morbidity and mortality associated with cachexia, mainstream treatment does not sustain weight and although nutritional supplements are commonly used, many of these have not been tested in clinical trials. Recent work in cachexia has revealed that this is mediated by pro-inflammatory cytokines. There are data that suggests that fish oils can affect the underlying pathogenic inflammatory response and have an affect on weight maintenance and nutritional balance

Diseases in which cachexia is most common:

Cancer
Chronic Heart Failure (CHF)
Chronic Obstructive Pulmonary Disease (COPD)
Rheumatoid Arthritis (RA)

Goals of the Study:

To evaluate the safety and efficacy of fish oils vs. corn oil in the maintenance of weight and lean body mass in patients with disease-related weight loss.
To understand the mechanism of fish oil effect on health maintenance by evaluating the anti-inflammatory, anti-catabolic, anti-oxidant and anabolic actions of these compounds
To document the effect of our interventions on quality of life and functional status.

Study Outline:

Participants will be randomly assigned to receive either fish oil supplements or corn oil for the duration of this 3-month study. Participants will have five study visits and two telephone interviews. During each study visit, participants will undergo laboratory tests, a physical exam, and a dual energy X-ray absorptiometry (DEXA) bone scan. Participants will be asked to keep a food diary during the study. During the telephone interviews, participants will be asked health-related questions and discuss their current functional status.

Enrollment

25 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Men and Women with disease-related weight loss e.g. cardiac cachexia, COPD, CHF, RA.
All stages of Pancreatic cancer patients (No weight loss requirements)
All stages of cancer with 5% weight loss
At least 6 weeks post-surgery
On a stable dose of medications for at least 6 weeks prior to study entry
Most recent ECOG Performance status score of 0,1,2,or 3 if applicable
Agree to use acceptable methods of contraception during the study and for 3 months after study completion, for female participants. Females with reproductive potential must have a negative urine or serum pregnancy test within 7 days of study.
Willing to continue current therapy for cancer for the duration of the study
If with diabetes mellitus HgbA1C of <10%
Adequate bone marrow function ANC> 1000/mm3, platelets 50,000/mm3, hemoglobin, 8g/dl.
No active infections including known history of HIV or viral hepatitis.

Exclusion criteria

Esophageal Cancer
Individuals with hypertriglyceridemia
Life expectancy of less than 12 weeks
Alcohol consumption more than 3 drinks/day for men or 2 drinks/day for women.
Untreated endocrine problems
Severe Depression
Untreated endocrine problems, such as hypothyroidism. Gonadal dysfunction from a known primary endocrine dysfunction (e.g. Klinefelters syndrome, pituitary tumor, testicular neoplasms, testicular surgery.
Medications that impair sex hormone synthesis, secretion, or function (e.g. spironolactone, anti-estrogens, anabolic steroids and androgens.
Fish oils within 3 months prior to study entry.
Any infectious disease, such as HIV or viral hepatitis.
Vitamins in doses greater than the Recommended Daily Allowance (RDA)
Herbs in the month prior to study entry.
Only participation in other cachexia studies is prohibited.
Prothrombin Time INR > 2.5 on Coumadin and INR > 2.0 not on Coumadin.