Clinical Trials Directory

Trials / Suspended

SuspendedNCT01567592

Extracorporeal Shockwave Therapy for the Treatment of Chronic Angina Pectoris

Clinical Trial Evaluating the Treatment of Patients With Refractory Angina Pectoris With Low Intensity Extracorporeal Shockwave Therapy Device

Status
Suspended
Phase
Phase 1
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Medispec · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Low intensity shockwaves have been proven in animal studies to induce local growth of new blood vessels from existing ones. The hypothesis of this study is that shockwave therapy could improve the symptoms of patients with refractory angina not amenable to revascularization with angioplasty or bypass surgery.

Detailed description

Low intensity shockwaves (1/10 the ones used in Lithotripsy) are delivered to myocardial ischemic tissue. Shockwaves are created by a special generator and are focused using a shockwave applicator device. The treatment is guided by standard echocardiography equipment. The shockwaves are delivered in synchronization with Patient R-wave to avoid arrhythmias. The treatment is painless. At first, the patient undergoes stress- SPECT testing to identify the ischemic areas. Following that, the same area is localized by the ultra-sound device and the shockwaves are focused to the ischemic area. Several treatments are required for optimal results.

Conditions

Interventions

TypeNameDescription
DEVICECardiac Extracorporeal Shockwave Therapy generator (Cardiospec)Energy Density - 0.09 mJ/mm2

Timeline

Start date
2009-03-01
Primary completion
2012-06-01
Completion
2012-12-01
First posted
2012-03-30
Last updated
2012-04-03

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01567592. Inclusion in this directory is not an endorsement.