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Trials / Unknown

UnknownNCT00955539

Viability and Cardiac Resynchronization Therapy

The Importance of Viability for Response to Cardiac Resynchronization Therapy

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
University Hospital, Gentofte, Copenhagen · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

30% of heart failure patients that receive a device for cardiac resynchronization therapy fail to show clinical improvement. The reason for lack of response is still unclear but factors such as scar tissue in the heart musculature, inadequate lead placement, device-settings and the degree of dyssynchrony before implant seems to be important. In this study, these factors are further investigated.

Detailed description

Cardiac resynchronization therapy (CRT) is an established therapy for patients with severe heart failure, depressed left ventricular function and a wide QRS-complex. Large clinical trials have demonstrated unequivocal improvements in functional status, morbidity and mortality. However, 30 % of heart failure patients treated with a CRT-device do not benefit clinically. Several factors have been suggested to be important for the response to CRT such as mechanical dyssynchrony, presence of scar tissue in the myocardium, and device-optimization (among others). It is the purpose of this study to investigate the importance of these factors. 100 patients with ischemic cardiomyopathy, eligible to CRT according to current guidelines, will be included. Patients are randomised to two arms. One group will have atrioventricular (AV)-optimization after implantation, the other AV -and interventricular (VV)-optimization. After 4 months patients are crossed-over to the other arm. Preimplantation patients are MR-scanned and low-dose dobutamine stress-echocardiography is performed. Furthermore patients will be examined by echocardiography and evaluation of clinical status 1. Mechanical dyssynchrony can predict response to CRT. b. Measures of mechanical dyssynchrony is related to myocardial viability and conduction. 2. Individual optimization based on conduction times will increase benefit to CRT. b. The effect of adding VV-optimization is related to myocardial viability. 3. \> 30 % of non-viable tissue globally in the myocardium is predictive of lack of CRT- response. b. Non-viable tissue located in the area of the left ventricular lead is predictive of non-response.

Conditions

Interventions

TypeNameDescription
DEVICEAV-optimization followed by AV- and VV-optimizationPatients are AV-optimized the first 4 months,then AV- and VV-optimized the next 4 months.
DEVICEAV- and VV-optimization followed by AV-optimization only.Patients are AV- and VV-optimized the first 4 months,then AV-optimized the next 4 months.

Timeline

Start date
2009-08-01
Primary completion
2012-12-01
Completion
2013-06-01
First posted
2009-08-10
Last updated
2011-10-06

Locations

2 sites across 2 countries: Denmark, Sweden

Source: ClinicalTrials.gov record NCT00955539. Inclusion in this directory is not an endorsement.