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Efficacy and safety of sucroferric oxyhydroxide on hemodialysis patients

Efficacy and safety of sucroferric oxyhydroxide on hemodialysis patients - Efficacy of sucroferric oxyhydroxide on HD

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000032867
Enrollment
60
Registered
2018-06-05
Start date
2016-01-06
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

Chronic kidney disease

Interventions

Sucroferric oxyhydroxide Lanthanum carbohydrate

Sponsors

Department of Nephrology, hypertension and Endocrinology, Nihon University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) age > 19 years and < 86 years, (2) hemodialysis duration >6 months at enrollment, and (3) hyperphosphatemia that was treated with lanthanum carbonate at least 12 weeks before enrollment.

Exclusion criteria

Exclusion criteria: (1) age < 20 years or > 85 years; (2) history of severe heart failure, angina, myocardial infarction, or stroke within the past 6 months; (3) presence of infectious disease, malignant tumors, or treatment with steroids or immunosuppressants; (4) current hospitalization; and (5) treatment with ferric citrate hydrate within the past 6 months.

Design outcomes

Primary

MeasureTime frame
FGF23 levels and anemia-related parameters

Secondary

MeasureTime frame
Ca, P, intact-PTH levels safety

Countries

Japan

Contacts

Public ContactTomoyasu Otsuki

Nihon University School of Medicine Nephrology, Hypertension and Endocrinology

totsuki16@gmail.com03-3972-8111

Outcome results

None listed

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