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Randomized, controlled trial of the clinical effect of selecrive SGLT2 blocker, ipragliflozin, and DPP-4 blocker in type 2 diabetic patients with NAFLD/NASH.- multicenter study -

Randomized, controlled trial of the clinical effect of selecrive SGLT2 blocker, ipragliflozin, and DPP-4 blocker in type 2 diabetic patients with NAFLD/NASH.- multicenter study - - Randomized, controlled trial of ipragliflozin and DPP-4 blocker in type 2 diabetic patients with NAFLD/NASH.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000015727
Enrollment
128
Registered
2014-11-24
Start date
2014-10-01
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

type 2 diabetic patients with NAFLD/NASH

Interventions

dietand ergotherapy and or (alpa-GI, Met) and sugra. diet and ergotherapy and/or (alpa-GI,Met) +DPP-4 blocker.

Sponsors

Saga University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Diet and exercise therapy plus or minus oral diabetes agent therapy, for example a-GI or metformin, for more than 12 weeks. The condition is the following HbA1c is more than 6.5 2.Patients with NASH or NAFLD diagnosed by using the guideline defined by JGH 3.Age is no fewer than 80, nor more than 20 4.Sex is female or male 5.Consenting patients

Exclusion criteria

Exclusion criteria: 1.Ppatients with diabetes 2.Patients with past history of ovascular lesion or stroke 3.Patients with past history of allergy 4.Patients with the necessity of IRI therapy 5.Patients with past history of liver disorder or renal dysfunction 6.Inadequacy of usingig this therapy

Design outcomes

Primary

MeasureTime frame
Rate of patients decreasing of HbA1c>0.5% and not gaining weight gain 72 weeks after administration.

Countries

Japan

Contacts

Public ContactHirokazu Takahashi

Saga University internal Medicine

takahas2@cc.saga-u.ac.jp0952-.34-2362

Outcome results

None listed

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