NCT00298441View on ClinicalTrials.gov

Efficacy of Intravenous Iron Administration in Hemodialysis Patients

PHASE4CompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

June 30, 2005

Primary Completion Date

May 31, 2006

Study Completion Date

March 31, 2007

Conditions
Chronic Renal FailureHemodialysisRenal AnemiaIron Deficiency Anemia
Interventions
DRUG

chondroitin sulfate-iron colloid

Trial Locations (2)

864-0033

Midorigaoka Clinic, Arao

860-8556

Kumamoto University Hospital, Kumamoto

All Listed Sponsors
lead

Kumamoto University

OTHER

NCT00298441 - Efficacy of Intravenous Iron Administration in Hemodialysis Patients | Biotech Hunter | Biotech Hunter