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Dose reduction in EP (Xres 3 vs Xres 4)

Dose reduction in EP (Xres 3 vs Xres 4) - Dose reduction in EP

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON37806
Enrollment
136
Registered
2012-04-06
Start date
2012-04-20
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

atrial fibrillation ventricular tachycardia

Interventions

None listed

Sponsors

Philips
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • Patients with heart rhythm disturbances undergoing an interventional treatment for their heart rhythm disturbance • Patients to be treated with ablation for atrial fibrillation (paroxysmal, persistent or permanent), atypical atrial flutter or patients to be treated with ablation for ischemic or non-ischemic ventricular tachycardia

Exclusion criteria

Exclusion criteria: • patients under 18 years of age

Design outcomes

Primary

MeasureTime frame
•Stochastic effect of X-ray dose expressed in Dose Area Product (DAP) •Deterministic effect of X-ray dose expressed in Air Kerma (AK)

Secondary

MeasureTime frame
• Staff dose measured by DoseAware and Electronic Personal Dosimeter (EPD) • Physician professional judgment on procedural success (yes/no) • Physician professional judgment on adequacy of images for performing the EP procedure (yes/no) • Procedure duration (measured as time between time of first puncture to time of catheter removal) • Fluoro and exposure times • Fluoro flavors

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)