| Trial ID: | L0488 |
| Source ID: | NCT06381076
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| Associated Drug: |
Liposomal Curcumin
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| Title: |
High-protein Oral Supplement With Liposomal Curcumin in Adults Undergoing Hemodialysis.
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| Acronym: |
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| Status: |
RECRUITING
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| Study Results: |
NO
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| Results: |
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| Conditions: |
Chronic Kidney Disease 5D
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| Interventions: |
DRUG: Liposomal curcumin|DRUG: Food colorant
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| 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
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| Sponsor/Collaborators: |
Sponsor: University of Florida
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| Gender: |
ALL
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| Age: |
ADULT, OLDER_ADULT
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| Phases: |
PHASE3
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| Enrollment: |
30
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| Study Type: |
INTERVENTIONAL
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| Study Designs: |
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: TREATMENT
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| Start Date: |
2025-02-03
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| Completion Date: |
2025-12
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| Results First Posted: |
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| Last Update Posted: |
2025-02-10
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| Locations: |
University of Florida, Gainesville, Florida, 32611, United States
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| URL: |
https://clinicaltrials.gov/show/NCT06381076
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