Strategic Management to Improve CRT Using Multi-Site Pacing Post Approval Study (Reference # C1918) (SMARTMSP)
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|ClinicalTrials.gov Identifier: NCT03257436|
Recruitment Status : Recruiting
First Posted : August 22, 2017
Last Update Posted : June 3, 2019
|Condition or disease||Intervention/treatment||Phase|
|Left Ventricular Dysfunction||Device: CRT-D||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||586 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Strategic Management to Improve CRT Using Multi-Site Pacing Post Approval Study (Reference # C1918)|
|Actual Study Start Date :||December 13, 2017|
|Estimated Primary Completion Date :||April 2020|
|Estimated Study Completion Date :||July 2020|
General population who receive a Boston Scientific Resonate family of CRT-D device in accordance with its labeled indication for use.
Left Ventricular MultiSite Pacing
- LV MSP feature [ Time Frame: Between 6 month visit and the 12 month visit in non-responders with LV MSP on for any duration. ]Related complication-free rate.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03257436
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