Measuring Hydration Levels of Healthy and Heart Failure Patients Before, During, and After an Electrophysiology (EP) Procedure
Cardiac Arrhythmia
About this trial
This is an interventional diagnostic trial for Cardiac Arrhythmia
Eligibility Criteria
Inclusion Criteria:
- Patients with cardiac arrhythmias or other cardiac conditions that are scheduled for EP procedures.
- Subject is over 18 years of age at the time of consenting
- Subject and/or legally authorized representative is willing to undergo the informed consent process prior to enrollment in the study
Exclusion Criteria:
- Pregnant subjects
- Subjects who are participating in another clinical study that may affect the results of either study
- Subjects who are unwilling or unable to wear the sensor for a period of up to 14 hours
- Subjects who are considered by the principle investigator to be medically unsuitable for study participation
Sites / Locations
- NYU Langone HealthRecruiting
Arms of the Study
Arm 1
Experimental
Hydrostasis group
50 study subjects scheduled for an EP procedure will have AleriTM sensors on subject's bicep, forearm, or wrist, to start data collection. Measurements will be made from the subject for a period of approximately 1 hours prior to the EP procedure. . Measurements will continue as patient is moved to the operating room. Once the EP procedure is complete, the subject will be transferred from the operating room to a hospital room, where they will stay overnight. Measurements will be made for 3-5hours post-operation.Detailed analysis will investigate how does AleriTM data correlate with known measures such as saline volume/rate, urine production volume, USG, Blood osmolality and body weight;