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Study identifier: NCT06687590 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Serranator POINT FORCE Registry

Condition: Peripheral Artery Disease (PAD) · Dysfunctional AV Fistula · Dysfunctional AV Graft  ·  Sponsor: Cagent Vascular LLC

PhaseN/A
Planned participants500
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The objective of this registry is to collect observational data under local standard of care and evaluate safety and performance of the Serranator® in treatment of peripheral artery disease (PAD), or dysfunctional native or synthetic arteriovenous dialysis fistulae in a real-world scenario. The data and conclusions derived from this study will be used to provide clinical evidence for the clinical evaluation process.

This description comes directly from the study's public registry record.

Talk to the study team

Alexis Shewfelt  ·  6502086743  ·  ashewfelt33@cagentvascular.com

Always discuss trial participation with your own doctor first.

Locations (19)

HonorHealthScottsdale, Arizona, United StatesRecruiting
Cedars-Sinai Medical CenterLos Angeles, California, United StatesRecruiting
Hartford HealthCareHartford, Connecticut, United StatesRecruiting
MedStar Washington Hospital / MedStar MontgomeryWashington D.C., District of Columbia, United StatesRecruiting
Manatee MemorialBradenton, Florida, United StatesRecruiting
Radiology and Imaging SpecialistsLakeland, Florida, United StatesRecruiting
Henry Ford HealthDetroit, Michigan, United StatesRecruiting
Barnes JewishSt Louis, Missouri, United StatesRecruiting
Atlantic Medical ImagingBrick, New Jersey, United StatesRecruiting
Virtua HealthMarlton, New Jersey, United StatesRecruiting
NorthwellNew Hyde Park, New York, United StatesRecruiting
Ohio State University Medical CenterColumbus, Ohio, United StatesRecruiting

+ 7 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06687590