BAROSTIM THERAPY™ In Heart Failure With Preserved Ejection Fraction
NCT: NCT02876042 · COMPLETED
Brief Summary
The purpose of this registry (NCT02876042) is to evaluate the effect of BAROSTIM THERAPY with the BAROSTIM NEO system in the commercial setting in subjects recently implanted under the CE-Marked indication for resistant hypertension that also have evidence of heart failure with preserved ejection fraction (HFpEF).
Frequently Asked Questions
What is BAROSTIM THERAPY™ In Heart Failure With Preserved Ejection Fraction?
BAROSTIM THERAPY™ In Heart Failure With Preserved Ejection Fraction is a clinical trial registered under NCT02876042. Current status: COMPLETED.
What is the status of NCT02876042?
The current status of NCT02876042 (BAROSTIM THERAPY™ In Heart Failure With Preserved Ejection Fraction) is: COMPLETED.
When did BAROSTIM THERAPY™ In Heart Failure With Preserved Ejection Fraction start?
BAROSTIM THERAPY™ In Heart Failure With Preserved Ejection Fraction started on 2017-03-23.
Related Devices
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.