At a glance
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A Pilot Study of Eicosapentaenoic Acid (EPA) in Patients With Cancer Cachexia
In Brief
A clinical study evaluating Eicosapentaenoic Acid for Cancer Cachexia. Completed, enrolled 36 participants across 2 sites.
Detailed Summary
The data collected through this pilot study will allow us to increase our understanding of cancer cachexia and the effect of Eicosapentaenoic Acid (EPA) on cancer cachexia. Our long-term goal is to improve nutritional treatment and reduce illness in the cancer patient population.
Study Details
Timeline
Interventions
Participants will receive Lovaza at a dose of 4 g for 6 weeks. Participants will be examined at six weeks for change in protein status as indicated by change in morphological (Height, weight, body mass index, body composition, lean body mass, body fat %), and biochemical (serum prealbumin) markers of protein status and immunological cytokines (Il-6, TNF- α) markers implicated in cancer cachexia. At baseline, 3 and 6 weeks, participants will undergo interviews and laboratory analysis for determining compliance and treatment-related toxicity.