CompletedNot Applicable

Patient Preferences for Leadless Pacemakers

United States117 participantsStarted 2022-03-28

Plain-language summary

Prospective, non-randomized, multi-center study designed to quantify patient preferences pertaining to risks and features of conventional transvenous pacemakers and leadless pacemakers

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

Mean Rankings for Pacemaker Device Features

Timeframe: Baseline

Results From RPL Model of Discrete Choice Experiment Choice Questions - Preference Weights (Effect-coded Parameters)

Timeframe: Baseline

Results From RPL Model of Discrete Choice Experiment Choice Questions- Standard Deviations

Timeframe: Baseline

Maximum-acceptable Risks of a Complication

Timeframe: Baseline

Maximum-acceptable Risks of an Infection

Timeframe: Baseline

Probability of Choosing Specified Pacemakers - All 3 Profiles

Timeframe: Baseline

Probability of Choosing Specified Pacemakers - Leadless Pacemaker Removable vs. Leadless Pacemaker Non-removable

Timeframe: Baseline

Probability of Choosing Specified Pacemakers - Leadless Pacemaker Removable vs. Pacemaker With Leads

Timeframe: Baseline

Trial details

NCT IDNCT05327101

SponsorAbbott Medical Devices

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2023-06-13

Results submitted2024-07-11

View on ClinicalTrials.gov More Cardiac Rhythm Disorder trials