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Use of "iSuite" During CMR-guided Electrophysiological Procedures

A

Academisch Ziekenhuis Maastricht

Status

Enrolling

Conditions

Cardiac Arrhythmia

Treatments

Other: Philips interventional MRI suite (Philips Healthcare, Best, the Netherlands)

Study type

Observational

Funder types

Other

Identifiers

NCT04727645
METC20-064 (Other Identifier)
NL74812.068.20

Details and patient eligibility

About

The perpuse of this study is to investigate the feasibility of the Philips interventional MRI suite "iSuite" to create an electroanatomical map of the heart based on which the real-time location of the catheters can be correctly and reliably visualized during CMR-guided electrophysiological procedure (CMR-EP).

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.
  • Contraindication for MRI such as: 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.

Trial contacts and locations

1

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Central trial contact

Miranda Bijvoet; Marisevi Chaldoupi

Data sourced from clinicaltrials.gov

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