Clinical Trials Directory

Trials / Completed

CompletedNCT02198495

Comparison Study of Two Iron Compounds for Treatment of Anemia in Hemodialysis Patients

Continuous Versus Periodic Intravenous Iron Supplementation in Maintenance Hemodialysis Patients

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
143 (actual)
Sponsor
Medical University of Vienna · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Patients with end-stage kidney disease on maintenance hemodialysis frequently require iron supplementation to compensate for ongoing iron losses, and to maintain hemoglobin levels with or without additional use of erythropoiesis-stimulating agents (ESA). The investigators aim to compare two different intravenous iron preparations, ferric carboxymaltose and iron sucrose in 140 hemodialysis patients. The investigators primary objective is to assess whether both agents are equally effective to maintain a target haemoglobin within 10-12 mg/dl. The investigators will also measure ferritin, transferrin, transferrin saturation, and how much ESA therapy is administered. Patients will be randomly assigned to either treatment group and followed in parallel over an active study period of 40 weeks.

Conditions

Interventions

TypeNameDescription
DRUGSupplementation of ferric carboxymaltose
DRUGSupplementation of iron sucrose

Timeline

Start date
2014-09-01
Primary completion
2019-05-01
Completion
2019-05-01
First posted
2014-07-23
Last updated
2020-09-11

Locations

2 sites across 1 country: Austria

Source: ClinicalTrials.gov record NCT02198495. Inclusion in this directory is not an endorsement.