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Changes in the factors associated with the renal prognosis during 12 months before and after administration of luseogliflozin in patients with type 2 diabetes

Changes in the factors associated with the renal prognosis during 12 months before and after administration of luseogliflozin in patients with type 2 diabetes - Changes in the factors associated with the renal prognosis during 12 months before and after administration of luseogliflozin in patients with type 2 diabetes

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000041193
Enrollment
200
Registered
2020-07-22
Start date
2018-11-01
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

diabetes mellitus

Interventions

None listed

Sponsors

Department of Diabetes, Metabolism and Kidney Disease,Edogawa Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with type 2 diabetes who were administered luseogliflozin

Exclusion criteria

Exclusion criteria: Subjects with replacement from other SGLT2 inhibitors or GLP-1 receptor antagonists, those with observation period less than 12 months, those with change of diuretics or anti-hypertensive agents during the observation period and those with add-on of GLP-1 receptor antagonists during the observation period

Design outcomes

Primary

MeasureTime frame
Changes in eGFR during 12 months before and after administration of luseogliflozin

Secondary

MeasureTime frame
Changes in urinary protein excretion, urinary albumin excretion and urinary L-FABP during 12 months after administration of luseogliflozin

Countries

Japan

Contacts

Public ContactHiroyuki Ito

Edogawa Hospital Department of Diabetes, Metabolism and Kidney Disease

ito@edogawa.or.jp03-3673-1221

Outcome results

None listed

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