High-protein Oral Supplement With Liposomal Curcumin in Adults Undergoing Hemodialysis.

3期 已完成 NCT06381076

摘要

A 12-week double-blind randomized control trial will be conducted among adults on hemodialysis (n=15) to determine the impact of liposomal curcumin in a high-protein product on inflammation markers and oxidative stress. Participants will be randomized via a computer-generator into either the control or intervention group. Participants in each group will be given a total of 38 g of a high protein product with or without 7 mls of liposomal curcumin for a total of 8 weeks. At baseline, weeks 8 and 12, participants will have blood sampled and complete a 3-day 24-hour recalls (2 non-dialysis days and 1 dialysis day) and a quality of life survey.

High-sensitivity C-reactive Protein

12 weeks or 84 days · milligrams per liter (mg/L)

在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文

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