Patient Preferences for Leadless Pacemakers
Status
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Details and patient eligibility
About
Prospective, non-randomized, multi-center study designed to quantify patient preferences pertaining to risks and features of conventional transvenous pacemakers and leadless pacemakers
Full description
The purpose of this study is to quantify patient preferences pertaining to risks and features of conventional transvenous pacemakers and leadless pacemakers. The preference study is designed to elicit patient preferences for risks and features that vary between a dual chamber leadless pacemaker system and a dual chamber transvenous pacemaker system, to quantify their relative importance.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- Able to read and speak English to consent to participate in the survey
- Willing and able to use a tablet or computer to complete the survey
- Scheduled to undergo evaluation for a de novo cardiac pacemaker at the study site (patient may or may not have a known indication for a pacemaker at the time)
Exclusion criteria
- None
Trial design
Trial contacts and locations
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Central trial contact
Grant Kim
Data sourced from clinicaltrials.gov
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