NL-OMON54396RecruitingNot Applicable
Prospective use of Philips *iSuite* electroanatomical mapping system in addition to standard CMR-guided electrophysiological procedures. - Use of iSuite during CMR-guided electrophysiological procedures.
Medisch Universitair Ziekenhuis Maastricht0 sites100 target enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Enrollment
- 100
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 18 to 99 (—)
Inclusion Criteria
- •- Already scheduled by the treating electrophysiologist for CMR-EP as standard
- •care for the treatment of a cardiac arrhythmia.
- •- Minimum age of 18 years old.
- •- Written informed consent.
Exclusion Criteria
- •- Participation in another investigational study that has not reached its
- •primary endpoint.
- •- Refusal of data storage until 15 years after end of study.
- •To be noted: All patients that are included in this study are already scheduled
- •and thus considered eligible for CMR-EP by the treating electrophysiologist. A
- •strict prerequisite for CMR-EP is that the patient has no contraindication for
- •MRI (metallic implant, body weight > 130 kg, pregnancy, breast feeding women,
- •known severe allergy to gadolineum contrast agents, renal failure with eGFR <=
- •30 mL/min/1,73m2) or contraindication for an EP procedure.
Investigators
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