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Clinical Trial Details

Trial ID: L0488
Source ID: NCT06381076
Associated Drug: Liposomal Curcumin
Title: High-protein Oral Supplement With Liposomal Curcumin in Adults Undergoing Hemodialysis.
Acronym:
Status: RECRUITING
Study Results: NO
Results:
Conditions: Chronic Kidney Disease 5D
Interventions: DRUG: Liposomal curcumin|DRUG: Food colorant
Outcome Measures: Primary: high-sensitivity C-reactive protein, baseline to end line in the concentration of high-sensitivity C-reactive protein between the control and intervention group., 12 weeks or 84 days | Secondary: Advanced glycation end products, baseline to end line in the concentration of advanced glycation end products between the control and intervention group., 12 weeks or 84 days|fatty acid byproduct - 4-hydroxynon-enal, baseline to end line in the concentration of fatty acid byproduct - 4-hydroxynon-enal between the control and intervention group., 12 weeks or 84 days|fatty acid byproduct - malondialdehyde, baseline to end line in the concentration of fatty acid byproduct - malondialdehyde between the control and intervention group., 12 weeks or 84 days|fatty acid byproduct - 8-F2 isoprostanes, baseline to end line in the concentration of fatty acid byproduct - 8-F2 isoprostanes between the control and intervention group., 12 weeks or 84 days|Klotho, baseline to end line in the concentration of klotho between the control and intervention group., 12 weeks or 84 days
Sponsor/Collaborators: Sponsor: University of Florida
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE3
Enrollment: 30
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: TREATMENT
Start Date: 2025-02-03
Completion Date: 2025-12
Results First Posted:
Last Update Posted: 2025-02-10
Locations: University of Florida, Gainesville, Florida, 32611, United States
URL: https://clinicaltrials.gov/show/NCT06381076