Proper Extent of Maze Intercaval Lesion
Withdrawn
- Conditions
- Atrial Fibrillation
- Registration Number
- NCT03091205
- Lead Sponsor
- Baylor Research Institute
- Brief Summary
It's hypothesized that a mean and range distance from the cavo-atrial junction to the area where there is complete loss of conductive tissue can be measured to better inform surgeons performing the Cox-Maze procedure. A patient scheduled for any cardiac surgery where visualization and mapping of cavo-atrial junction is possible could be entered into the study if they meet the inclusion/exclusion requirements.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
- Age ≥ 18 years male or female
- Scheduled for any cardiac surgery where visualization and mapping of cavo-atrial junction is possible
- Subjects willing and able to provide written informed consent
Exclusion Criteria
- Subjects receiving surgery with non-sternotomy access
- Presence of or history of transvenous pacing leads
- Subjects receiving a re-do cardiac surgery
- Subjects with a history of pericarditis
- Subjects who are in atrial fibrillation or atrial flutter and cannot be converted out of it.
- Any medical condition or finding for which the Investigator used medical discretion to determine the subject should be excluded
- Subject is currently participating in another clinical trial.
- Subject is unable to provide written informed consent.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Distance until complete loss of conductive tissue 6 Months To measure the mean and range distance from the cavo-atrial junction to the area where there is complete loss of conductive tissue.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
The Heart Hospital Baylor Plano
🇺🇸Plano, Texas, United States
The Heart Hospital Baylor Plano🇺🇸Plano, Texas, United States