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Effect of a DPP-4 inhibitor on left ventricular diastolic dysfunction in patients with type 2 diabetes and diabetic cardiomyopathy

Effect of a DPP-4 inhibitor on left ventricular diastolic dysfunction in patients with type 2 diabetes and diabetic cardiomyopathy - Effect of a DPP-4 inhibitor on left ventricular diastolic dysfunction (3D)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000003784
Enrollment
120
Registered
2010-10-01
Start date
2010-10-01
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

Type 2 diabetic patients with left ventricular diastolic dysfunction

Interventions

Sponsors

Cardiovascular Dysfunction Study group
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1, T2DM patients those who have been treated with the diabetic therapy and whose blood glucose has not been sufficiently controlled 2, The patients with left ventricular diastolic dysfunction LVEF>50% e'< 8 cm/s and/or E/e'>15 3, Obtaining written informed consent

Exclusion criteria

Exclusion criteria: 1, The patient under insulin treatment 2, The patient under alpha-GI or Gulinide treatment 3, Severe ketosis, diabetic coma, or precoma within the past six months 4, Severe infectious disease, pre/ post operation or serious injury 5, Type 1 diabetes mellitus 6, Insufficiently controlled diabetes mellitus (HbA1c >= 9.0% ) 7, Insufficiently controlled hypertension (SBP>=160mmHg) 8, Myocardial infarction or stroke within 6 months before recruiting 9, LV hypertrophy (LV wall thickness > 13mm) 10, The patient with atrial fibrillation 11, The patient with significant valvular disease 12, Women who are pregnant, possibly pregnant, or are breastfeeding 13, Mild renal dysfunction (sCr>=1.5 mg/dl) 14, Hypersensitivity or allergy to sitagliptin and voglibose 15, Patients who are determined by the investigators to be unsuitable

Design outcomes

Primary

MeasureTime frame
Change in e' and e'/E after 24 weeks

Countries

Japan

Contacts

Public ContactNaoko Fujimoto

Cardiovascular Dysfunction Study group Research Secretariat Office

edge.3d@n-place.co.jp03-3814-1616

Outcome results

None listed

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