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NCT04051541 · ClinicalTrials.gov registry record · NA
Simulation of Adenosine Push Methods for Treatment of SVT Using Agitated Saline Visualized by Ultrasound
A NA study of Supraventricular Tachycardia, sponsored by HealthPartners Institute.
- Completed
- Registry status
- NA
- Development phase
- 20
- Enrollment target
- 1
- Study location
NCT04051541: Completed NA study of Supraventricular Tachycardia, sponsored by HealthPartners Institute.
NCT04051541 is a NA study of Supraventricular Tachycardia that has completed, run by HealthPartners Institute. The registered enrollment target is 20 participants, below the 124-participant average among 3 other Supraventricular Tachycardia trials with a reported enrollment target (84% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04051541, a NA study of Supraventricular Tachycardia, has completed, sponsored by HealthPartners Institute.
- COMPLETED
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
Supraventricular tachycardia (SVT) is an abnormally fast heart rhythm arising from improper electrical activity in the upper part of the heart. SVT is commonly treated with adenosine using three different IV administration techniques. However, it is not well known which of these three techniques is the quickest or most likely to reach the heart in order to stop SVT. This study will simulate each of those techniques in an investigator-blinded procedure. Intravenous agitated saline, used as a surrogate for a dose of adenosine, will be administered to healthy volunteers using all three techniques and monitored using bedside ultrasound to observe their efficacy and speed in reaching the right side of the heart.
Primary Outcome
Time from IV push to ultrasound visualization of agitated saline in the right heart
Conditions Studied
Interventions
- OTHER Agitated saline push
Study Locations (1)
Minnesota
- Regions Hospital - Saint Paul
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2019-05-06 |
| Est. Completion | 2019-06-28 |
| Phase | NA |
What the finished NCT04051541 record still lists
NCT04051541 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 124-participant average among 3 other Supraventricular Tachycardia trials with a reported enrollment target (84% lower).
The record links to 1 condition, with Supraventricular Tachycardia appearing as the primary indexed condition, and to 1 intervention - of which Agitated saline push is the first listed.
NCT04051541 reports a single indexed study location in Minnesota.
Frequently Asked Questions
What is clinical trial NCT04051541 about?
NCT04051541 is a clinical study titled "Simulation of Adenosine Push Methods for Treatment of SVT Using Agitated Saline Visualized by Ultrasound". Supraventricular tachycardia (SVT) is an abnormally fast heart rhythm arising from improper electrical activity in the upper part of the heart. SVT is commonly treated with adenosine using three different IV administration techniques. However, it is not well known which of these three techniques is ...
What is the current status of trial NCT04051541?
This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2019-05-06. Estimated completion is 2019-06-28.
What conditions does trial NCT04051541 study?
This clinical trial studies the following conditions: Supraventricular Tachycardia.
What interventions are being tested in trial NCT04051541?
The interventions under investigation include: Agitated saline push (OTHER).
Who is sponsoring clinical trial NCT04051541?
This trial is sponsored by HealthPartners Institute, which has 146 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04051541 being conducted?
This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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