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Clinical Trial Details

Trial ID: L0609
Source ID: NCT05544513
Associated Drug: Ferrous Sulfate 3 Days Week
Title: Oral Iron Supplementation for Patients With Chronic Kidney Disease
Acronym:
Status: ACTIVE_NOT_RECRUITING
Study Results: NO
Results:
Conditions: Chronic Renal Disease|Iron-Deficiency Anemia|Anemia of Chronic Kidney Disease|Dysbiosis
Interventions: DRUG: Ferrous sulfate 3 days week|DRUG: Ferrous sulfate daily|DRUG: Ferrous sulfate higher concentration
Outcome Measures: Primary: Change in cytokines plasma levels measured by ELISA after supplementation with oral iron, cytokines plasma levels, 2 months | Secondary: Change in uremic toxin plasma levels after supplementation with oral iron, Get blood samples to evaluate the supplementation effects in uremic toxins such as indoxyl sulfate, p-cresyl sulfate, 2 months
Sponsor/Collaborators: Sponsor: Universidade Federal Fluminense
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE2
Enrollment: 6
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: SINGLE (PARTICIPANT)|Primary Purpose: TREATMENT
Start Date: 2022-08-01
Completion Date: 2026-12-30
Results First Posted:
Last Update Posted: 2025-04-03
Locations: Denise Mafra, Rio de Janeiro, RJ, 22260050, Brazil
URL: https://clinicaltrials.gov/show/NCT05544513