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NCT02154750 · ClinicalTrials.gov registry record · NA
AV Delay Optimization vs. Intrinsic Conduction in Pacemaker Patients With Long PR Intervals
A NA study of Cardiac Arrhythmia and Atrioventricular Block, sponsored by University of California, San Diego.
- Completed
- Registry status
- NA
- Development phase
- 23
- Enrollment target
- 1
- Study location
NCT02154750 is a NA study of Cardiac Arrhythmia and Atrioventricular Block that has completed, run by University of California, San Diego. The registered enrollment target is 23 participants, below the 211-participant average among 12 other Cardiac Arrhythmia trials with a reported enrollment target (89% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02154750, a NA study of Cardiac Arrhythmia and Atrioventricular Block, has completed, sponsored by University of California, San Diego.
- COMPLETED
- Registry status
- NA
- Development phase
- 23 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a randomized, prospective clinical trial to determine the effects of two different pacemaker atrioventricular delay (AV delay) settings on heart function in patients with dual chamber pacemakers implanted for symptomatic bradycardia with long PR intervals (delayed conduction between upper and lower chambers of the heart). The study will compare a long, fixed AV delay (standard) with an optimized AV delay for each individual using echocardiography (experimental).
Conditions Studied
Interventions
- DEVICE Long, fixed AV delay
- DEVICE Short, optimized AV delay
Study Locations (1)
California
- UCSD Sulpizio Cardiovascular Center - La Jolla
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 23 participants |
| Start Date | 2013-06-01 |
| Est. Completion | 2021-12-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02154750
The ClinicalTrials.gov registry entry for NCT02154750 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 23 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 211-participant average among 12 other Cardiac Arrhythmia trials with a reported enrollment target (89% lower). The listed sponsor is University of California, San Diego, which has 775 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Cardiac Arrhythmia appearing as the primary indexed condition, and to 2 interventions - of which Long, fixed AV delay is the first listed.
NCT02154750 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT02154750 about?
NCT02154750 is a clinical study titled "AV Delay Optimization vs. Intrinsic Conduction in Pacemaker Patients With Long PR Intervals". This is a randomized, prospective clinical trial to determine the effects of two different pacemaker atrioventricular delay (AV delay) settings on heart function in patients with dual chamber pacemakers implanted for symptomatic bradycardia with long PR intervals (delayed conduction between upper an...
What is the current status of trial NCT02154750?
This trial is currently completed. It is a NA study. The enrollment target is 23 participants. The study started on 2013-06-01. Estimated completion is 2021-12-31.
What conditions does trial NCT02154750 study?
This clinical trial studies the following conditions: Cardiac Arrhythmia, Atrioventricular Block, Sick Sinus Syndrome, Symptomatic Bradycardia.
What interventions are being tested in trial NCT02154750?
The interventions under investigation include: Long, fixed AV delay (DEVICE), Short, optimized AV delay (DEVICE).
Who is sponsoring clinical trial NCT02154750?
This trial is sponsored by University of California, San Diego, which has 775 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02154750 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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