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Confirm Rx Insertable Cardiac Monitor SMART Registry

N/A
Waitlist Available
Led By Fabio Quartieri, MD
Research Sponsored by Abbott Medical Devices
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group

Summary

The purpose of the Confirm Rx SMART Registry is to collect real world data to assess the safety and performance of the Confirm Rx Insertable Cardiac Monitor (ICM) and system over a 12 month period. A sub-set of subjects enrolled in the Confirm Rx SMART Registry will meet the Post Market Clinical Follow-Up (PMCF) requirement for CE mark.

Eligible Conditions
  • Atrial Fibrillation
  • Arrhythmia
  • Symptoms

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Find a Location

Who is running the clinical trial?

Abbott Medical DevicesLead Sponsor
652 Previous Clinical Trials
415,011 Total Patients Enrolled
77 Trials studying Atrial Fibrillation
30,689 Patients Enrolled for Atrial Fibrillation
Fabio Quartieri, MDPrincipal InvestigatorArcispedale S. Maria Nuova - IRCCS l
~238 spots leftby Jan 2026
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