Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Intersection Medical, Inc.
The implanted CRM device will have shock therapy and rate sensor temporarily deactivated or placed in magnet mode during the time the IMED-4 is activated. The IMED-4 will be activated for a time not to exceed 15 minutes. During the time the IMED-4 is active, the CRM device programmer will print the voltage sensing of the implanted lead in real-time. The printout will be examined for the presence of far-field sensing artifacts.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Subjects with an active implantable CRM device
Subjects \> 18 years of age
Subjects who are ambulatory not requiring assistance for ambulation
Subjects who have been informed of the nature of the study and agree to its provisions and have provided written informed consent as approved by the IRB
You may not be if
Subjects who are pregnant or lactating or who have been pregnant within the past three months
Subjects who have tattoos on the back in the electrode patch placement region
Subjects who have had a past allergic reaction to adhesives
Subjects who have poor general physical/mental health that, in the opinion of the investigator, will not allow the subject to be a good study candidate (i.e. other disease processes, mental capacity, substance abuse, shortened life expectance, etc.)
Clareo Health | Observational Study of ICD and Pacemaker Sensing in the Presence of IMED-4 Operation
