Geneva, Aug. 29 -- International Clinical Trials Registry received information related to the study (NCT07129421) titled 'Evaluation of Safety and Effectiveness of the EMBLOK EPS Compared With No Cerebral Embolic Protection During TAVR' on Aug. 4.
Study Type: Interventional
Study Design:
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Prevention. Masking: Single (Outcomes Assessor).
Primary Sponsor: Emblok, Inc.
Condition:
AORTIC VALVE DISEASES
Aortic Valve Stenosis and/or Insufficiency
Aortic Valve Regurgitation
Aortic Valve Replacement
Intervention:
Device: EMBLOK™ Embolic Protection System ("EMBLOK EPS")
Recruitment Status: Not recruiting
Phase: N/A
Date of First Enrollment: October ...