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Effect of polaprezinc vs zinc acetate dihydrate in Patients Receiving Hemodialysis With Zn deficiency; a single center, open label, randomized clinical study

Effect of polaprezinc vs zinc acetate dihydrate in Patients Receiving Hemodialysis With Zn deficiency; a single center, open label, randomized clinical study - Effect of polaprezinc vs zinc acetate dihydrate in Patients Receiving Hemodialysis With Zn deficiency; a single center, open label, randomized clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000031200
Enrollment
110
Registered
2018-02-08
Start date
2018-04-11
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients on maintenance hemodialysis with zinc deficiency

Interventions

zinc acetate dihydrate 25mg twice a day, for 24 weeks Polaprezinc 75mg twice a day, for 24 weeks

Sponsors

Hirosaki University Graduate School of Medicine
Lead Sponsor
Oyokyo Kidney Research Institute Aomori Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Hemodialysis patients, hemodialysis vintage >6months, with serum levels of zinc <70 microgram/dL 2.Age of >20 years old 3. Patients who are able to understand contents of this trial and give written informed consents

Exclusion criteria

Exclusion criteria: 1. Hemodialysis vintage of <6 months 2. Already priscribed polaprenzinc or zinc acetate dihydrate 3. Unwillingness to participate in the study 4. Recent active infection 5. End stage of malignancy 6. Previous history of blood transfusion within at least 3 months before the trial 7. Severe liver damage 8. Drug/alcohol abuse 9. Patients who are not appropriate for the tial

Design outcomes

Primary

MeasureTime frame
The cahnge in the serum levels of zinc 6 months after the trial

Secondary

MeasureTime frame
The change in Erythropoeisis stimulant agent resistance 6 months after the trial The change in the serum levels of copper 6 months after the trial

Countries

Japan

Contacts

Public ContactShingo Hatakeyama

Dept. of Urology, Hirosaki University Graduate School of Medicine Department of Urology

shingorilla2@gmail.com0172395091

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026