Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Medtronic Cardiac Rhythm and Heart Failure
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Patient is indicated for continuous arrhythmia monitoring with an Insertable Cardiac Monitor (ICM)
Patient is willing to undergo implant in clinic setting with only local anesthetic and/or oral anti-anxiety medications for sedation
Patient is 18 years of age or older
Patient is willing and able to provide consent and authorize the use and disclosure of health information
Patient is willing and able to comply with the protocol including the required follow-up
You may not be if
Patient has reduced immune function or is otherwise at high risk for infection
Patient has had a recent (within 30 days) or otherwise unresolved infection
Patient is implanted or indicated for implant with a pacemaker, Implantable Cardioverter-Defibrillator (ICD), Cardiac Resynchronization Therapy (CRT), or hemodynamic monitoring system
Patient is participating in another clinical study that may have an impact on the study endpoints
Patient's life expectancy is less than 1 year
Patient is pregnant
Patient has unusual thoracic anatomy or scarring at the implant site which may adversely affect the success of the implant procedure
