Skip to content

Ozempic Retrospective study, Investigation from real-world data of GLP-1 receptor Agonist, semaglutide, Multicenter trial In Japan

Ozempic Retrospective study, Investigation from real-world data of GLP-1 receptor Agonist, semaglutide, Multicenter trial In Japan - ORIGAMI study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000050499
Enrollment
700
Registered
2023-03-06
Start date
2023-03-06
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

type 2 diabetes mellitus

Interventions

None listed

Sponsors

Toho University Omori Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who meet all of the following criteria are included in this study; 1. Patients with type 2 diabetes mellitus 2. Patients who used Ozempic at least once till 2022/6/30 3. Patients aged 18 years or older at the initiation of this study (at approval by institutional review board)

Exclusion criteria

Exclusion criteria: Patients who fall into any of the following criteria are excluded from participating in the study; 1. Patients with type 1 diabetes mellitus 2. Patients with excessive drinking of alcohol (net alcohol intake is more than 60g/day for male or 30g/day for female) 3. Patients with dementia 4. Patients who were pregnant during data collection period 5. Patients who were hospitalized for a week or longer within 52 weeks after the initial date 6. Patients with poor medication adherence (judged by attending physician) 7. Patients with other conditions that the attending physician think inappropriate to participate in the study

Design outcomes

Primary

MeasureTime frame
Change in HbA1c

Secondary

MeasureTime frame
Change or percent change in the following items; - Major blood tests - Other general blood tests - vital signs

Countries

Japan

Contacts

Public ContactArata Yoneda

EviPRO Co., Ltd. EviPRO Co., Ltd.

yoneda_arata@evipro.co.jp03-3255-8286

Outcome results

None listed

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