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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03388385
Other study ID # 10488/19.04.2016
Secondary ID
Status Active, not recruiting
Phase Phase 4
First received
Last updated
Start date September 20, 2017
Est. completion date December 20, 2022

Study information

Verified date August 2022
Source Carol Davila University of Medicine and Pharmacy
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the effects of acute intravenous iron administration on the endothelial function in non-dialysis Chronic Kidney Disease stages G3-G5 patients with anemia and iron deficiency, in relation to changes in oxidative and nitrosative status.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 40
Est. completion date December 20, 2022
Est. primary completion date December 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Chronic kidney disease stages G3-G5 (defined according to KDIGO criteria); - Anemia (defined according to KDIGO criteria) and iron deficiency defined as serum ferritin < 100 ng/mL and/or TSAT < 20% (KDIGO). Exclusion Criteria: - contraindications of intravenous iron therapy: iron allergy, active infection, hemochromatosis, iron overload (serum ferritin > 500 ng/mL and/or transferrin saturation > 50%); - treatment with iron and erythropoiesis-stimulating agents (at the time of recruitment and 6 months previously); - active smoker status; - antioxidant food supplements treatment in the last 3 months; - clinically manifest bleeding; - another cause of anemia (hemoglobinopathies, vitamin B12 and/or folic acid deficiency suggested by the megaloblastic peripheral blood smears's appearance, multiple myeloma and other paraproteinemias); - severe anemia (Hb < 7 g/dl); - baseline FMD < 7% (the existence of atherosclerosis which limits arterial reactivity); - cancer (currently or in the past 6 months); - hepatopathies (increased serum transaminases = 3 x normal value) or hepatic impairment = grade Child B; - autoimmune disorders or significant inflammation (as defined by C-reactive protein > 5 mg/L); - pregnancy or lactation; - participation in other clinical trials over the upast 3 months; - patient unwillingness.

Study Design


Intervention

Drug:
Sodium Chloride 0.9% Intravenous Solution
Physiologic saline infusion will be infused in day 1.
Ferinject
Ferric carboxymaltose will be infused in day 2.

Locations

Country Name City State
Romania "Dr. Carol Davila" Teaching Hospital of Nephrology Bucharest

Sponsors (2)

Lead Sponsor Collaborator
Carol Davila University of Medicine and Pharmacy S.C. Sanador S.R.L

Country where clinical trial is conducted

Romania, 

Outcome

Type Measure Description Time frame Safety issue
Primary Effect on endothelial function Description of the endothelial function variation (changing in flow-mediated vasodilatation (FMD) endothelium-dependent, and also in serum sICAM-1, sVCAM-1 and nitric oxide metabolism parameters ) after administration of a single intravenous dose of iron versus a control solution, in CKD non-dialysis patients. through study completion, an average of 1 year
Primary Oxidative stress Description of some free radicals production's markers (lipid peroxidation and carbonyl stress assessment) and in antioxidant system in plasma markers variation after administration of a single intravenous iron dose versus a control solution, in non-dialysis CKD subjects. through study completion, an average of 1 year
Secondary Correlation between endothelial dysfunction and oxidative stress markers Evaluation of correlations between changes in oxidative stress parameters and endothelial function after a single intravenous iron administration compared to a control solution in non-dialysis CKD subjects. through study completion, an average of 1 year
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