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The effects of Teneligliptin on vascular inflammatory markers in post-PCI (Percutaneous Coronary Intervention) patients.

The effects of Teneligliptin on vascular inflammatory markers in post-PCI (Percutaneous Coronary Intervention) patients. - The effects of Teneligliptin on vascular inflammatory markers in post-PCI (Percutaneous Coronary Intervention) patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000027224
Enrollment
20
Registered
2017-05-02
Start date
2017-04-03
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

Coronary Artery Disease

Interventions

Additional treatment of Teneligliptin Conventional treatment

Sponsors

Kameda Medhical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Elective PCI patients 2)Patients who have T2DM and HbA1c (NGSP) level are more than 7% before PCI 3)Patients aged 30 up to 80 years old 4)Informed consent was signed by all patients and documented.

Exclusion criteria

Exclusion criteria: 1)Patients with T1DM (type 1 diabetes mellitus) 2)Patients who have medical history of hypersensitivity to diabetes mellitus drugs 3)Patients with medical history of malignant tumor 4)Patients with severe infection, before and after operation, or severe trauma 5)Patients with cardiac arrest (class of III in NYHA) 6)Patients with uncontrolled hypertension 7)Patients with insulin dependent and the potential to change diabetic drugs 8)Patients with severe renal insufficiency (eGFR is less than 30 mL / min / 1.73 m2, dialysis-dependent, or serum creatinine (men, more than 2.5 mg / dL, women, more than 2.0 mg / dL 9) Patients with pregnant, and possibly pregnant 10) Patients with severe ketosis, diabetic coma, or history of coma within the past six months 11)Patients who had stroke, cerebral hemorrhage, subarachnoid hemorrhage, or transient ischemic attack within the past three months. 12)Patients who enrolled into another clinical test within three months prior to this trial 13)Patients who cannot administer antiplatelet drugs 14)Patients who were considered as inappropriate for the study by the investigator.

Design outcomes

Primary

MeasureTime frame
Variation amount and rate of inflammatory markers from pretreatment levels.

Secondary

MeasureTime frame
Vascular endothelial function: RH-PAT score, variation amount and rate of HbA1c, and glucose from pretreatment levels.

Countries

Japan

Contacts

Public ContactAya JUNI

AsMediX Co., Ltd. GPO Department , Business Planning Section

aya_juni@asmedix.co.jp03-6230-3661

Outcome results

None listed

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