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N/A Completed N=74 Randomized Treatment

Using Non-Fluoroscopic Imaging Devices to Decrease Radiation Exposure During Ablation of Supraventricular Tachycardia

Source: ClinicalTrials.gov NCT00979303 ↗
Enrolled (actual)
74
Serious AEs
0.0%
Results posted
Mar 2018
Primary outcomePrimary: Total Fluoroscopy Time — 18.3; 7.5 minutes

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.

Outcome Measures

OutcomeResultp-value
PRIMARY
Total Fluoroscopy Time
18.3; 7.5
SECONDARY
Total Radiation Exposure
387; 110

Eligibility Criteria

Inclusion Criteria

  • Age >/=8
  • Weight >/=25kg
  • Structurally normal heart (no major cardiac defects)
  • History of SVT
  • No prior history of cardiac surgery or ablation

Exclusion Criteria

  • Congenital Heart Disease
  • Prior history of cardiac surgery or ablation
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00979303). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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