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Study of FIrst-liNE STrategy for obese TYpe2 DiabetEs in Dokkyo Saitama

FINEST TYDES - FINEST TYDES

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000045234
Enrollment
300
Registered
2021-09-01
Start date
2020-12-23
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

type2 diabetes mellitus(DM)

Interventions

SGLT2 inhibitor DPP4 inhibitor

Sponsors

Dokkyo Medical University Saitama Medical Center Department of Diabetes, Endocrinology and Hematology
Lead Sponsor
Dokkyo Medical University
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Obese T2DM patients(age 20-75) 2)Drug-naive patients or those to whom oral hypoglycemic agents have been discontinued more than 1 year before consent. 3) The outpatients of Dokkyo Medical University Saitama Medical Center. 4) Patients for whom consent is obtained in writing to be enrolled in the current study.

Exclusion criteria

Exclusion criteria: 1) The patients treated with oral hypoglycemic agents currently or within one year. 2) Patients who are pregnant or may be pregnant. 3)Patients with serious complications such as heart diseases, liver diseases, and kidney disorder. 4) Patients judged to be inappropriate as a participant by doctors

Design outcomes

Primary

MeasureTime frame
HbA1c (up to 12 months from the start of administration)

Secondary

MeasureTime frame
BP. BW, BMI, sCPR, CBC, AST,ALT, gGTP, TP, Cr, BUN, UA,Na, K, Cl, FBS, T-Chol, HDL-C, LDL-C, TG, Ketone bodies, urine(u)-glucose , u-occult blood, u-ketone bodies.

Countries

Japan

Contacts

Public ContactKoshi Hashimoto

Dokkyo Medical University Saitama Medical Center Department of Diabetes, Endocrinology and Hematology

k-hashi@dokkyomed.ac.jp+81-48-965-1111

Outcome results

None listed

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