CAPTURE-2: Controlled Arterial Protection to Ultimately Remove Embolic Material

Part of paid clinical trials in New Orleans, Louisiana.

Sponsor
EmStop Inc
Study ID
NCT07276711
Status
Recruiting

Conditions

  • Aortic Stenosis
  • Aortic Valve Disease
  • Aortic Valve Stenosis

Eligibility Criteria

Sex
ALL
Age
22 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • EmStop Embolic Protection System — DEVICE
    EmStop Embolic Protection System used during TAVR procedure
  • Boston Scientific Sentinel — DEVICE
    Sentinel device used during TAVR procedure

Study Details

The objective of this study is to demonstrate safety and efficacy of the EmStop Embolic Protection System when used as indicated to capture and remove thrombus/debris during self-expanding transcatheter aortic valve replacement (TAVR) procedures.

Key Dates

Start date
May 12, 2026
Status verified
May 2026
Primary completion
May 31, 2028
Completion
May 31, 2028

Study Design

Enrollment
663 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: EmStop System
  • Active Comparator: Boston Scientific Sentinel device

Primary Outcome Measure

Non-Inferiority [ Time Frame: Non-inferiority of 30-day EmStop device MACCE patient incidence rate compared to the Sentinel device patient incidence rate ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
Ochsner Medical CenterNew OrleansLouisiana70121
James S Jenkins, MD (PRINCIPAL_INVESTIGATOR)
Mission HealthAshevilleNorth Carolina28801
Michaeal Chenier, MD (PRINCIPAL_INVESTIGATOR)

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