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Iron Therapy in Patients With End-Stage Renal Disease

K

Kaohsiung Medical University

Status

Unknown

Conditions

Anemia
Inflammation
Cardiovascular Risk Factor
End-stage Renal Disease

Treatments

Drug: irone sucrose

Study type

Interventional

Funder types

Other

Identifiers

NCT04491916
KMUHIRB-F(I)-20190110

Details and patient eligibility

About

This study will compare the clinical outcome of patients with maintenance dialysis room after changing the iron treatment guidelines from original upper limit with ferritin>500ng/ml, or TSAT>20% to Ferritin> 800ng / ml, or TSAT> 50%.

Full description

After two years of treatments, we will compare the incidence of clinical events, monthly blood, and biochemical examination data for the two years before and after the change.

Enrollment

200 estimated patients

Sex

All

Ages

20 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients receiving maintenance dialysis

Exclusion criteria

  • less than 20 year-old, oncological patients undergoing chemotherapy, abnormal liver function, infection

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

200 participants in 1 patient group

Iron Treatment
Experimental group
Description:
Treatment with iron sucrose with orginal guideline from ferritin\>500ng/ml, or TSAT\>20% to ferritin\>800ng/ml, or TSAT\>50%.
Treatment:
Drug: irone sucrose

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Hugo Y Lin, MD, PhD

Data sourced from clinicaltrials.gov

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