Skip to content

n-3 Polyunsaturated Fatty Acids in Obesity

Impact of n-3 Polyunsaturated Fatty Acids on Adipose Tissue Inflammation in Morbidly Obese Patients

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00760760
Acronym
PUFA-ATI
Enrollment
55
Registered
2008-09-26
Start date
2008-09-30
Completion date
2016-03-31
Last updated
2016-03-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adipose Tissue Inflammation, Morbid Obesity

Brief summary

Inflammation in the adipose (fat) tissue is an important condition leading to metabolic derangements and cardiovascular disease in obese patients. n-3 polyunsaturated fatty acids exert anti-inflammatory effects and prevent adipose tissue inflammation in rodent obesity. This study tests the hypothesis that n-3 polyunsaturated fatty acids ameliorate adipose tissue inflammation in morbidly obese patients.

Interventions

DRUGreesterified long-chain n-3 polyunsaturated fatty acids (EPA, DHA)

4g daily, 8 weeks

DRUGcontrol

equivalent amount of fat as butter

Sponsors

National Bank of Austria
CollaboratorOTHER_GOV
Medical University of Vienna
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Non-diabetic morbidly obese patients (BMI \> 40 kg/m2) supposed to undergo bariatric surgery * Age 20-65 yrs

Exclusion criteria

* Acute illness within the last two week * Known diabetes mellitus or current anti-diabetic medication * Acquired immunodeficiency (HIV infection) * Hepatitis or other significant liver disease * Severe or untreated cardiovascular, renal, pulmonary disease * Untreated or inadequately treated clinically significant thyroid disease * Anemia * Active malignant disease * Inborn or acquired bleeding disorder including warfarin treatment * Pregnancy or breast feeding * Drug intolerability that prohibits the use of the study drug

Design outcomes

Primary

MeasureTime frame
Adipose tissue inflammationEight weeks of treatment

Secondary

MeasureTime frame
Metabolic controlEight weeks of treatment
Dependence of effects on Pparg polymorphismsEight weeks of treatment

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 25, 2026