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Completed

NCT Number: NCT01754506

Testing Fish Oil Derivatives In Healing Of Chronic Venous Leg Ulcers

The purpose of this study is to test the efficacy of an oral, nutrient intervention containing the bioactive components of fish oil to promote healing of chronic venous leg ulcers (CVLU). If this systemic, nutrient intervention is found to alter the microenvironment of CVLU, the science of wound healing and care of patients with CVLU will be vastly improved.

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Ohio State University College of Nursing

Columbus, Ohio, 43210, United States

About this study

The pathogenesis of CVLU involves high numbers of activated polymorphonuclear leukocytes (PMN) that are associated with persistent inflammation in the wound bed 5-9. We propose to test the efficacy of an oral, nutrient intervention containing the bioactive components of fish oil to assuage PMN activity and promote healing of CVLU. If this systemic, nutrient intervention is found to alter the microenvironment of CVLU, the science of wound healing and care of patients with CVLU will be vastly improved.

The purpose of this study is to test three fundamental corollaries of our organizing hypothesis in a 2-group, double-blind, randomized, experimental design on CVLU patients. The findings from the proposed experiments will increase our understanding of lipid mediators that influence wound healing and PMN function, and may lead to an innovative approach to reduce the physical and emotional burdens of nonhealing or recurrent CVLU.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • men and women
  • ages 18-85 years
  • having at least one existing CVLU between the ankle and knee for ≥ 3 months
  • medical clearance to take 81mg/d of aspirin
  • prescribed compression therapy; ambulatory
  • ankle brachial pressure index (ABPI) of ≥ 0.8
  • target wound of ≥ 1 x 1 inches (6.25 cm2)
  • can understand English and sign own consent

Exclusion criteria

  • allergy to fish or seafood
  • exposed bone, tendon or fascia around target wound
  • receiving warfarin or Plavix therapy
  • immunologic related condition (e.g. Crohn's disease, systemic lupus erythematosus)
  • chronic inflammatory skin diseases (e.g. pyoderma gangrenosum, psoriasis)
  • requiring non-steroidal anti-inflammatory drugs > 2x a week
  • nutritional supplements or corticosteroids
  • chronic renal insufficiency
  • already in a study related to CVLU.

Treatment and study plan

Fish Oil

Dietary Supplement

EPA + DHA Group subjects (n=54) will be given n-3 fatty acid supplement softgels

Primary outcomes

  1. Levels of eicosapentaenoic (EPA)+ docosahexaenoic (DHA)-derived lipid mediators and proinflammatory cytokines in blood and CVLU wound fluid

    Time frame: 0, 28, 56 days

Secondary outcomes

  1. PMN counts and levels of PMN-derived proteases in CVLU wound fluid

    Time frame: 0, 28, 56 days

Other outcomes

  1. Re-epithelialization

    Time frame: 28, 56 days

Sponsors and collaborators

Lead sponsor

Ohio State University

Other

Collaborators

  • National Institute of Nursing Research (NINR)

Registry information

Important dates

Study start
2013
Primary completion
2015
Study completion
2015
First posted
Dec 21, 2012
Registry last updated
Oct 16, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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