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. Author manuscript; available in PMC: 2017 Jan 6.
Published in final edited form as: J Interv Card Electrophysiol. 2013 Dec 3;39(3):287–294. doi: 10.1007/s10840-013-9845-z

Table 3.

Summary of clinical trials of ECWT for the treatment of ischemic heart disease

Trial Patients (number) Patient population Trial type CCS class NTG use (per week) EF (%) 6MWT (meters) NYHA class Nuclear imaging outcomes
Fukumoto, et al. 2006 (26) 9 End-stage CAD Series 2.7 to 1.8** 5.4 to 0.3* n/a n/a n/a Improved SSS* but not SRS (NS) by stress thallium scan
Gutersohn, et al. 2006 (29) 14 End-stage CAD Series 3.4 to 2.4 *** n/a n/a n/a n/a Improved perfusion by SPECT
Kikuchi, et al. 2010 (27) 8 End-stage CAD Randomized, placebo-controlled, cross-overa 3.0 to 2.3** 4.1 to 0.9** 51 to 56* 200 to 330** n/a n/a
Vasyuk, et al. 2010 (28) 24 Ischemic cardiomyopathy (EF<40 %) Seriesb 2.6 to 1.9 ** n/a 32 to 38* 414 to 538** 2.2 to 1.7** Improved SRS* and SSS* by stress SPECT
Wang, et al. 2010 (30) 25 (and 10 controls) CAD with chronic stable angina Case–control Improved Improved n/a Improved Improved* Improved perfusion on rest SPECT**
Peng, et al. 2012 (31) 50 Ischemic cardiomyopathy Randomized, placebo-controlledc Improved** Improved** 45 to 47** Improved* Improved** Improved perfusion** and viability* on rest SPECT/PET
Yang, et al. 2012 (32) 25 CAD without prior revascularization Randomized, placebo-controlledc 2.0 to 1.0* 2.0 to 1.0** 51 to 56* 383 to 438* 2.0 to 1.0* Improved perfusion*** and viability** on rest SPECT/PET

CCS Canadian Cardiovascular Society (angina class), NTG nitroglycerine, EF ejection fraction, 6MWT 6-minute walk test, NYHA New York Heart Association, CAD coronary artery disease, NS p >0.05, SSS summed stress score, SRS summed rest score, SPECT single photon emission computed tomography, PET positron emission tomography

*

p <0.05

**

p <0.01

***

p <0.001

a

No significant change in endpoints pre- and post-treatment in control group

b

No significant change in endpoints pre- and post-placebo treatment

c

Comparison of all endpoints between post-treatment ECWT and placebo groups p <0.05