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NCT00979303 · ClinicalTrials.gov registry record · NA
Using Non-Fluoroscopic Imaging Devices to Decrease Radiation Exposure During Ablation of Supraventricular Tachycardia
A NA study, sponsored by Boston Children's Hospital.
- Completed
- Registry status
- NA
- Development phase
- 74
- Enrollment target
NCT00979303: Completed NA study, sponsored by Boston Children's Hospital.
NCT00979303 is a NA study that has completed, run by Boston Children's Hospital. The registered enrollment target is 74 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00979303, a NA study, has completed, sponsored by Boston Children's Hospital.
- COMPLETED
- Registry status
- NA
- Development phase
- 74 participants
- Enrollment target
Study Summary
The purpose of this study is to determine whether the additional use of non-fluoroscopic imaging modalities can decrease the use of radiation exposure during standard ablation procedures for supraventricular tachycardia (SVT) in children.
Primary Outcome
Total fluoroscopy time in minutes
Interventions
- DEVICE Intracardiac echocardiography and 3D navigational system
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 74 participants |
| Start Date | 2009-01-09 |
| Est. Completion | 2010-05-28 |
| Phase | NA |
What the finished NCT00979303 record still lists
NCT00979303 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 74 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).
The record links to 0 conditions, and to 1 intervention - of which Intracardiac echocardiography and 3D navigational system is the first listed.
NCT00979303 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00979303 about?
NCT00979303 is a clinical study titled "Using Non-Fluoroscopic Imaging Devices to Decrease Radiation Exposure During Ablation of Supraventricular Tachycardia". The purpose of this study is to determine whether the additional use of non-fluoroscopic imaging modalities can decrease the use of radiation exposure during standard ablation procedures for supraventricular tachycardia (SVT) in children.
What is the current status of trial NCT00979303?
This trial is currently completed. It is a NA study. The enrollment target is 74 participants. The study started on 2009-01-09. Estimated completion is 2010-05-28.
What interventions are being tested in trial NCT00979303?
The interventions under investigation include: Intracardiac echocardiography and 3D navigational system (DEVICE).
Who is sponsoring clinical trial NCT00979303?
This trial is sponsored by Boston Children's Hospital, which has 462 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00979303's enrollment target sits among peer trials
74 1082nd of 2000 higher than 912 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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