MedPath

Periodic Versus Continuous IV Iron Supplementation in HD Patients

Phase 4
Completed
Conditions
Anemia of Chronic Kidney Disease
Interventions
Registration Number
NCT02787824
Lead Sponsor
Papageorgiou General Hospital
Brief Summary

The purpose of this study was to compare the efficacy of two regimens of intravenous iron sucrose \[continuous (in every hemodialysis session) versus intermittent (every 1-4 weeks)\] on the response of rHuEPO in the maintenance phase of its administration in hemodialysis patients.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
27
Inclusion Criteria
  • Constant rHu-EPO and iron dose for at least 2 months before starting the study
  • Hemoglobin ≥ 8,5g/dl and <12,5 g/dl
  • Ferritin < 1000 mg/dl
  • TSAT < 50%
  • CRP < 5 mg/dl
Exclusion Criteria
  • Malignant tumor disease
  • Oral iron supplementation
  • Active bleeding issues
  • Surgical intervention within the last 8 weeks before study inclusion

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
continuous iv administration of iron sucroseIron Sucrose SupplementPrior to the study, all our patients were receiving intravenous iron sucrose in an intermittent mode (every 1-4 weeks).Patients on this arm will receive the same previous dose of iron glucose but in a continuous mode (smaller doses of iron sucrose in every session).
intermittent iv administration of iron sucroseIron Sucrose SupplementPatients on this arm will continue to receive the same previous intermittent mode of iron sucrose.
Primary Outcome Measures
NameTimeMethod
Change of serum hemoglobin level (g/dl)Month 0, 1, 2, 3, 4
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Papageorgiou General Hospital

🇬🇷

Thessaloniki, Greece

© Copyright 2025. All Rights Reserved by MedPath