Skip to content

Assessment of endothelium-dependent hyperpolarization in patients with microvascular and/or vasospastic angina

Assessment of endothelium-dependent hyperpolarization in patients with microvascular and/or vasospastic angina - Assessment of endothelium-dependent hyperpolarization in patients with microvascular and/or vasospastic angina

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000030269
Enrollment
130
Registered
2017-12-15
Start date
2017-12-20
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

Microvascular angina Vasospastic angina

Interventions

Aspirin 486 mg
L-NMMA acetate 8 micromol/min for 5 minutes
bradykinin acetate 25 ng/min, 50 ng/min and 100 ng/min for 2 minutes each, 3 times
nitroglycerin 0.3 mg sublingual administration. Four times measurement of FMD and RH-PAT.

Sponsors

Department of Cardiovascular Medicine, Tohoku University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ?Patients who are hospitalized for being suspected microvascular and/or coronary vasospastic angina by catheterization, or our outpatients diagnosed with microvascular and/or coronary vasospastic angina. ?Regardless of gender.

Exclusion criteria

Exclusion criteria: ?Patients in hospital due to acute coronary syndrome. ?Patients with cardiogenic shock or heart failure. ?Patients with end-stage renal failure with internal shunt. ?Patients taking continuous intravenous infusion of cardiovascular agents such as inotropes and vasodilators. ?Patients who have resting systolic blood pressure below 100 mmHg or more than 200mmHg at the time of measurement of endothelial functions. ?Patients who have arrhythmia such as atrial fibrillation and are considered to be difficult to measure vascular endothelial function. ?Patients with a history of aspirin asthma. ?Patients who are taking any antithrombotic therapies except single antiplatelet agent. ?Patients who are pregnant or have a possibility of pregnancy, and who are falling within 28 days after childbirth or breast-feeding ?Patients are considered to be difficult to participate in the trial due to mental illness or psychiatric symptoms. ?Patients who are judged to be inappropriate for participating in the study by us.

Design outcomes

Primary

MeasureTime frame
Endothelial functions as evaluated by FMD (flow-mediated dilation) and RH-PAT (reactive hyperemia-peripheral arterial tonometry).

Secondary

MeasureTime frame
Endothelial function-related biomarkers such as NOx, adiponectin, Rho-kinase activity, ADMA (asymmetric dimethylarginine).

Countries

Japan

Contacts

Public ContactShoko Kajitani

Tohoku University Graduate School of Medicine Cardiovascular Medicine

shoko_k0520@cardio.med.tohoku.ac.jp0227177153

Outcome results

None listed

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