A Random Selection of Patients From the SENTRY Study Who Have a Bioconverted Sentry IVC Filter in Situ With a Minimum Dwell Time of 24 Months From a Single Center Follow up

NC Heart and Vascular Research, LLC

Status: Completed

Conditions: Recurrent Pulmonary Embolism (Disorder)

Treatments: Diagnostic Test: IVUS

Study type: Observational

Funder types: Other

Identifiers

NCT04208139

Version 1.0

Details and patient eligibility

About

IVUS Evaluation of the Bioabsorbable Sentry IVC Filter 3-5 Years Post Deployment Follow up

Full description

IVUS Evaluation of the Bioabsorbable Sentry IVC Filter 3-5 Years Post Deployment Follow up

Enrollment: 11 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 18 years of age
• Signed the informed consent document
• Participants from the SENTRY clinical trial willing to undergo one time IVUS evaluation ( outpatient )

Exclusion criteria

• Any filter that remained non converted.