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The improvement effect of liver dysfanction and inhibitory effect of fibrosis marker by sitagliptin or repaglinide treatment for fatty liver(liver dysfunction) patients with type2 diabetes mellitus.

The improvement effect of liver dysfanction and inhibitory effect of fibrosis marker by sitagliptin or repaglinide treatment for fatty liver(liver dysfunction) patients with type2 diabetes mellitus. - The improvement effect of liver dysfanction and inhibitory effect of fibrosis marker by sitagliptin or repaglinide treatment for fatty liver(liver dysfunction) patients with type2 diabetes mellitus.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000012513
Enrollment
50
Registered
2014-12-07
Start date
2012-07-02
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 Liver dysfunction

Interventions

Group A: sitagliptin 50mg QD Group B: repaglinide 0.25mg TID

Sponsors

Osaka Medical College Hospital
Lead Sponsor
Osaka Medical College Hospital, Ishikiriseiki Hospital, Shiroyama Hospital, Sugimoto Clinic, Seikeikai Hospital, Taisyou Hospital, First Towakai Hospital, Hanwasumiyosi General Hospital, Hokusetsu General Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patients who have fatty liver by picture evaluation ( abdomen echo check, abdomen CT inspection) 2)Patients who have abnormalities in AST, ALT, or gamma-GTP 3)Patients who have abnormalities in TG, T-CHO, or FFA 4)Patient who have abnormalities in either IV type collagen S or ferritin Patients who fulfilled above 1) and 2)as indispensable condition, and either 3) or 4), or both 3) and 4)

Exclusion criteria

Exclusion criteria: 1) Patients who have renal dysfunction 2) Patients whose medicine or its dosage changed during the study duration if antihypertensive drug, antilipidemial drug or medicine which effects on other liver functions is used. 3) Patients who are considered inappropriate as a target patient by a physician-in-charge

Design outcomes

Primary

MeasureTime frame
NAFIC score(Ferritin, IRI, Type4collagen 7s)

Secondary

MeasureTime frame
diagnostic imaging, blood test , adiponecti, GLP-1(Active form), free fatty acid

Countries

Japan

Contacts

Public ContactShinya Fukunishi

Osaka Medical College Hospital Second internal medicine

in2104@ph.osaka-med.ac.jp072-683-1211

Outcome results

None listed

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