Phase
Condition
Pain (Pediatric)
Inflammation
Treatment
Fucoidan extracted from U. Pinnatifida
Fucoidan extracted from U. Pinnatifida
Fucoidan extracted from F. Vesiculosus
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Survivors of cancer
Age 18 or older
Speak and understand English
Have completed surgery, radiation, and/or systemic intravenous anticancer therapy (e.g., chemotherapy, targeted therapy, immunotherapy) ≤10 years prior to enrollment.
Have a baseline level of fatigue, as determined by reporting a score of 4 or higherfor the question, "In the last week, how bad was your worst fatigue on a scale from 0-10?"
Be willing to commit to the fucoidan supplement dosing and delivery method, tocomplete evaluation instruments, and to attend all study visits.
Completed Informed Consent
Exclusion
Exclusion Criteria:
Current warfarin or other anti-coagulation medication use.
Current use of supplements that contain fucoidan
Any allergy to fucoidan
Be diagnosed with a major psychiatric illness requiring hospitalization within thelast year.
Be diagnosed with dementia.
Be pregnant or nursing
Study Design
Connect with a study center
University of Rochester Medical Center
Rochester, New York 14642
United StatesSite Not Available
University of Rochester Medical Center
Rochester 5134086, New York 5128638 14642
United StatesActive - Recruiting
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