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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 is a clinical trial that has completed, run by Baylor Research Institute. The registered enrollment target is 30 participants.
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.
Interventions
- DEVICE Permanent Pacemaker Placement
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2015-01 |
| Est. Completion | 2019-12-20 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02994667
The ClinicalTrials.gov registry entry for NCT02994667 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Baylor Research Institute, which has 180 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Permanent Pacemaker Placement is the first listed.
NCT02994667 reports 0 study locations.
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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