Skip to content

Liraglutide reduce infarction size in a acute myocardiac infarction patients with Diabetes mellitus

Liraglutide reduce infarction size in a acute myocardiac infarction patients with Diabetes mellitus - LISA Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005687
Enrollment
100
Registered
2011-06-01
Start date
2011-06-01
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

Diabetes mellitus acute myocardiac infarction

Interventions

Liraglutide Placebo

Sponsors

Shin-Tokyo hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: he case that was treated for myocardial infarction to assume the left coronary arteries Diabetes which have already received a diabetes drugs or the person which became the diagnosis of diabetes during hospitalization The person who does not receive GLP-1 analog and the DPP-IV inhibitor so far

Exclusion criteria

Exclusion criteria: Case having a serious renal damage and liver damage(Cr>2.0mg/dl, T-Bil>3.0mg/dl, PT<60%, Alb<2.8mg/dl) CABG enforcement planned case Case within CABG enforcement three months Case contraindicated to the dosage of Liraflutide The case that is using insulin Case having a serious underlying disease (including a malignant tumor, an infectious disease, DIC) The case that infarction responsibility blood vessel is a bypass graft

Design outcomes

Primary

MeasureTime frame
Improvement degree of cardiac function expressed in EF(Teichholz method , Simpson method) and EDV at start of therapy, one week later, the time of a discharge, six months later

Secondary

MeasureTime frame
1. Change of the following item RBC, WBC, Hb, Ht, Plt, TC, LDL-C, TG, HDL-C, ALT, AST, ganma-GTP, CK, CK-MB, BUN, Cr, BS, HbA1c, 1,5-AG, BNP 2. Coronary angiography (QCA:Quantitative Coronary Analysis) at the time of start of therapy, before a discharge, six months later . 3.Improvement degree of cardiac function expressed by MRI 4.major adverse cardiac events 5.Hypoglycemia event

Countries

Japan

Contacts

Public Contactkoji sakai

Shin-Tokyo hospital Endocrinolory and diabetes internal medicine

kojisakai@sc4.so-net.ne.jp+81-47-366-7000

Outcome results

None listed

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