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NCT02994667 · ClinicalTrials.gov registry record
Pacemaker Utilization and Ventricular Pacing in Patients Undergoing Trans-catheter Aortic Valve Replacement (TAVR)
A clinical trial, sponsored by Baylor Research Institute.
- Completed
- Registry status
- 30
- Enrollment target
NCT02994667: Completed study, sponsored by Baylor Research Institute.
NCT02994667 is a clinical trial that has completed, run by Baylor Research Institute. The registered enrollment target is 30 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02994667 has completed, sponsored by Baylor Research Institute.
- COMPLETED
- Registry status
- 30 participants
- Enrollment target
Study Summary
The purpose of this study is to assess the incidence (at 90-days) of ventricular pacing in patients undergoing permanent pacemaker placement after TAVR. As well as incidence (at 90-days) of atrioventricular block (AVB), intraventricular conduction delay (IVCD), bundle branch block (BBB), and rate histogram in patients undergoing permanent pacemaker placement after TAVR.
Primary Outcome
Incidence of Ventricular pacing post permanent pacemaker placement after TAVR as indicated by Pacemaker interrogation or remote monitoring system.
Interventions
- DEVICE Permanent Pacemaker Placement
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2015-01 |
| Est. Completion | 2019-12-20 |
What the finished NCT02994667 record still lists
NCT02994667 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 30 participants, a relatively small participant target.
The record links to 0 conditions, and to 1 intervention - of which Permanent Pacemaker Placement is the first listed.
NCT02994667 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02994667 about?
NCT02994667 is a clinical study titled "Pacemaker Utilization and Ventricular Pacing in Patients Undergoing Trans-catheter Aortic Valve Replacement (TAVR)". The purpose of this study is to assess the incidence (at 90-days) of ventricular pacing in patients undergoing permanent pacemaker placement after TAVR. As well as incidence (at 90-days) of atrioventricular block (AVB), intraventricular conduction delay (IVCD), bundle branch block (BBB), and rate h...
What is the current status of trial NCT02994667?
This trial is currently completed. The enrollment target is 30 participants. The study started on 2015-01. Estimated completion is 2019-12-20.
What interventions are being tested in trial NCT02994667?
The interventions under investigation include: Permanent Pacemaker Placement (DEVICE).
Who is sponsoring clinical trial NCT02994667?
This trial is sponsored by Baylor Research Institute, which has 180 total clinical trials registered on ClinicalTrials.gov.
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