Clinical Trial

Functional Proteomics of Uremic Retention Solutes Associated With Immunosenescence, Inflammation and Impaired Adaptive Stress Response

Active, Not Recruiting
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Summary
This is a randomized controlled crossover trial (58) in order to characterize PBL damage and death rate in hemodialysis patients treated with membranes with different permeability, including protein-leaking dialysers. The study will enroll fourty patients on regular 4-h three times per week hemodialysis (HD) of the dialysis unit of the "Fondazione IRCCS Policlinico San Matteo" (Pavia, Italy). Thirteen age and sex matched healthy individuals (Ctr) and ten CKD patients on peritoneal dialysis treatment (PD\*) will be included as healthy and CKD-matched controls, respectively. Comparison between HD and PD patients is aimed to assess the effect of biocompatibility and protein leakage during the treatments
Trial Details
NCT Number NCT07265635
Lead Sponsor Fondazione IRCCS Policlinico San Matteo di Pavia
Conditions Hemodialysis
Enrollment 30 participants
Start Date 2025-02-17
Primary Completion 2027-02-17 (estimated)
Study Completion 2027-02-17 (estimated)
Updated on ClinicalTrials.gov 2025-12-05