NCT Number: NCT01066078
Echocardiography and Peak Endocardial Acceleration (PEA) Measurements in Cardiac Resynchronization Therapy (CRT)
This study used an external endocardial acceleration sensor (sonR sensor), placed on the patient's chest, to time the closure of aortic and mitral valves, and compared its performance with echocardiography.
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Notify MeKey information
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Primary location
Nouvelles Cliniques Nantaises, Nantes, France
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Every patient coming in the participating centers for an echocardiographic exam and implanted with a pacemaker or an implantable cardioverter defibrillator (ICD) can be included in the study.
Exclusion criteria
- Inability to understand the patient information sheet.
- Minor patient or pregnant woman.
Treatment and study plan
Primary outcomes
-
The timings of mitral (tMC) and aortic (tAC) valves closure by echocardiography and sonR
Time frame: 12 months
Sponsors and collaborators
Lead sponsor
LivaNova
Industry
Registry information
Official study title
Echocardiography and PEA Measurements in CRT Therapy
Important dates
- Study start
- 2007
- Primary completion
- 2009
- Study completion
- 2009
- First posted
- Feb 10, 2010
- Registry last updated
- Mar 5, 2010
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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