● Recruiting

Post-market Surveillance of Micorport CRM Cardiac Implantable Electronic Devices

Condition: Cardiac Rhythm Disorder · Heart Failure · Sudden Cardiac Death · Sponsor: MicroPort CRM

PhaseN/A

Planned participants2500

Who can joinAll sexes, 18 Years to 90 Years

Healthy volunteersNo

About this study

The primary objective of the study is to assess the chronic safety of MicroPort CRM market-released systems.

This description comes directly from the study's public registry record.

Talk to the study team

Hanan FAWAZ, MSC · 33616531960 · hanan.fawaz@crm.microport.com

Always discuss trial participation with your own doctor first.

Locations (1)

Hospital Santa Marta Lisboa

Lisbon, Portugal

Recruiting

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Source record: clinicaltrials.gov/study/NCT05694572