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Clinical Trials/NL-OMON54396
NL-OMON54396
Recruiting
Not 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:
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ConditionsCardiac arrhythmiacardiac heart rhythm disturbance.10007521

Overview

Phase
Not Applicable
Status
Recruiting
Sponsor
Medisch Universitair Ziekenhuis Maastricht
Enrollment
100
OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational non invasive

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

Sponsor
Medisch Universitair Ziekenhuis Maastricht

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