Evaluation of Safety and Efficacy of the Mynx Control Venous Vascular Closure Device 6F-12F vs Manual Compression

NACompletedINTERVENTIONAL
Enrollment

352

Participants

Timeline

Start Date

August 30, 2022

Primary Completion Date

July 11, 2023

Study Completion Date

July 11, 2023

Conditions
Venous Vascular Closure
Interventions
DEVICE

MYNX CONTROL™ Venous Vascular Closure Device 6F-12F

Mynx Control Venous VCD 6F-12F is indicated for use to seal femoral venous access sites while reducing times to hemostasis and ambulation.

Trial Locations (14)

27607

NC Heart and Vascular Research, Raleigh

28277

OnSite Clinical Solutions, Rock Hill

33176

Baptist Health Miami Cardiac and Vascular Institute, Miami

33312

Palm Vascular Centers, Miami Beach

33614

Tampa Cardiovascular Interventions and Research, Tampa

37403

Erlanger Health System, Chattanooga

64111

Saint Luke's Hospital of Kansas City, Kansas City

73134

Hightower Clinical, Oklahoma City

73135

South Oklahoma Heart Research, Oklahoma City

75069

North Dallas Research Associates, McKinney

75230

Medical City Dallas Hospital, Dallas

78503

Rio Grande Regional Hospital, McAllen

80228

Colorado Heart and Vascular PC, Lakewood

85016

Arizona Cardiovascular Research Center, Phoenix

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

NAMSA

OTHER

lead

Cordis Corporation

INDUSTRY

NCT05554471 - Evaluation of Safety and Efficacy of the Mynx Control Venous Vascular Closure Device 6F-12F vs Manual Compression | Biotech Hunter | Biotech Hunter