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Low-energy extracorporeal cardiac shock wave therapy in patients with severe ischemic heart disease

Low-energy extracorporeal cardiac shock wave therapy in patients with severe ischemic heart disease - Shock wave therapy for ischemic heart disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000011484
Enrollment
5
Registered
2013-09-01
Start date
2013-09-01
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

Angina pectoris

Interventions

Sponsors

chibanishi general hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Men and women 20 years of age or older. 2) Patients who have chest pain even under standard medication. 3) Patients with no indication of revascularization (PCI or CABG), or patients in whom eonugh improvement is not expected compared to the risk of revascularization. 4) Canadian Cardiovascular Society (CCS) classification, Class II-IV patients. 5) Evidence of myocardial ischemia with myocardial stress-scintigraphy or stress MRI

Exclusion criteria

Exclusion criteria: 1) Patients whose target area cannot be observed with echocardiography. 2) Post-breast augmentation surgery with silicon pad. 3) Patients with prosthetic valve (mechanical valve) in the heart. 4) Q-wave myocardial infarction within 3 months. 5) Non-Q-wave myocardial infarction within 6 weeks. 6) Less than 1 month after the last revascularization (PCI or CABG). 7) Patients with cardiogenic shock or worsening heart failure (who require continuous infusion of cardiovascular agents such as inotropic agents or vasodilators). 8) Intracardiac thrombus. 9) Patients whose clinical status changed after the last coronary angiography. 10) Unstable diabetic retinopathy. 11) Patients who have malignancy or who have undergone surgery because of malignancy within the past five years

Design outcomes

Primary

MeasureTime frame
Frequency in use of nitroglycerin per week. Evaluated at 3 month after the therapy.

Secondary

MeasureTime frame
CCS class scores, Exercise tolerance, Myocardial perfusion. Evaluated at 3 month after the therapy.

Countries

Japan

Outcome results

None listed

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