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Liraglutide Effect and Action in Diabetes: Evaluation of Cardiovascular Outcome Results Trial in Japan

Liraglutide Effect and Action in Diabetes: Evaluation of Cardiovascular Outcome Results Trial in Japan - READ

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000006817
Enrollment
20
Registered
2011-12-01
Start date
2011-05-01
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

ACS patient with type II diabetes

Interventions

Liraglutide will be administrated to the patients with type 2 diabetes within 14 days of onset of ACS. It will be continued for 6 months.

Sponsors

Department of Cardiovascular Medicine, Saga University
Lead Sponsor
Shinkoga hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: For entry into the study, participants must meet all of the following criteria. (1) Aged 20 and over (Gender: regardless) (2) type II diabetes (3)Patients who are hospitalized for ACS such as cardiac infarction, unstable angina. (within 14days of onset) (4)Patient with full understanding of this study and agrees with written consent. The agreement must be based on the patients' free will.

Exclusion criteria

Exclusion criteria: Exclusion criteria:patients will be excluded from the study when they meet to any of the criteria. (1)patients with cardiogenic shock (2)patient with serious liver disease((AST)GOT/(ALT)GPT>100) (3)patient with serious kidney trouble.(Cre>5mg/dl and patients under dialysis) (4)Patients with a past history of drug allergy and hypersensitivity. (5)Pregnant and/or breast-feeding at present,or a woman of child-bearing potential. (6)Patients with malignant neoplasms (7)Iinsulin-requiring diabetics.(Type 1,or type 2 with depletion of insulin secretion capacity.) (8)patients who was diagnosed that his/her condition is not appropriate to join this study.

Design outcomes

Primary

MeasureTime frame
(1)Biomarker of cardiovascular disease (NT-proBNP,high sensitive troponin T,hs-CRP,MCP-1,eGFR,cystatinC,(S)-RAGE,MDA-LDL,AIM,etc) and shift of UACR (2)Changes in left ventricular function (left ventricular ejection rate, left ventricular volume, diastolic function)(3)change in HbA1c,FBS (4)safeness

Countries

Japan

Contacts

Public ContactKoichi Node, MD. PhD.

Saga University Department of Cardiovascular Medicine

node@cc.saga-u.ac.jp0952-34-2364

Outcome results

None listed

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