# Efficacy of Intravenous Iron Administration in Hemodialysis Patients

> **NCT00298441** · PHASE4 · COMPLETED · sponsor: **Kumamoto University** · enrollment: 50 (—)

## Conditions studied

- Chronic Renal Failure
- Hemodialysis
- Renal Anemia
- Iron Deficiency Anemia

## Interventions

- **DRUG:** chondroitin sulfate-iron colloid

## Key facts

- **NCT ID:** NCT00298441
- **Lead sponsor:** Kumamoto University
- **Sponsor class:** OTHER
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2005-06
- **Primary completion:** 2006-05
- **Final completion:** 2007-03
- **Target enrollment:** 50 (—)
- **Last updated:** 2008-05-12


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00298441

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00298441, "Efficacy of Intravenous Iron Administration in Hemodialysis Patients". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT00298441. Licensed CC0.

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