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Clinical Trial Details

Trial ID: L0288
Source ID: NCT06794593
Associated Drug: Camostat Mesylate
Title: Effect Camostat for Kidney Protection in Chronic Kidney Disease
Acronym: CamKid
Status: RECRUITING
Study Results: NO
Results:
Conditions: Chronic Kidney Disease(CKD)
Interventions: DRUG: Camostat Mesylate
Outcome Measures: Primary: 24 h Urine sodium excretion (mmol/day), At baseline (day 0), before treatment with IMP (day 5), and after completion of 4 days treatment with IMP (day 9).|Water excretion (L), 24 h urine collection, At baseline (day 0), before treatment with IMP (day 5), and after completion of 4 days treatment with IMP (day 9).|Total Body Water (L), Measured by Body Composition Monistor, At baseline (day 0), before treatment with IMP (day 5), and after completion of 4 days treatment with IMP (day 9).|Home blood pressure, At baseline (day 0), before treatment with IMP (day 5), and after completion of 4 days treatment with IMP (day 9). | Secondary: Urine protease activity: zymography + protease activity, At baseline (day 0), before treatment with IMP (day 5), and after completion of 4 days treatment with IMP (day 9).|Tubular complement activation, Urine C3a, MAC-sC5b-9, C3dg, MBL, At baseline (day 0), before treatment with IMP (day 5), and after completion of 4 days treatment with IMP (day 9).|Urine microvesicles: gammaENaC cleavage, At baseline (day 0), before treatment with IMP (day 5), and after completion of 4 days treatment with IMP (day 9).|Urine microvesicles: complement deposition, At baseline (day 0), before treatment with IMP (day 5), and after completion of 4 days treatment with IMP (day 9).|24 hours urine albumin excretion (mg/day), At baseline (day 0), before treatment with IMP (day 5), and after completion of 4 days treatment with IMP (day 9).|Plasma concentration of renin, NT-proBNP, angiotensin II and aldosterone, At baseline (day 0), before treatment with IMP (day 5), and after completion of 4 days treatment with IMP (day 9).
Sponsor/Collaborators: Sponsor: Odense University Hospital
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE2
Enrollment: 40
Study Type: INTERVENTIONAL
Study Designs: Allocation: NON_RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2024-11-21
Completion Date: 2027-02-28
Results First Posted:
Last Update Posted: 2025-01-27
Locations: Department of Nephrology, Odense University Hospital, Odense, 5000, Denmark
URL: https://clinicaltrials.gov/show/NCT06794593