US Post-Market Surveillance Study of the Surfacer System

Recruiting now

Conditions studied: Venous Disease

In brief

Single arm, observational, multi-center, consecutively enrolling, post-market surveillance study. Treating patients in need of central venous access who have upper body venous occlusions or other conditions that preclude central venous access by conventional methods, and who meet the requirements described in the device labeling.

Key facts

Study ID

NCT05050799

Run by

Merit Medical Systems, Inc.

People needed

30

Starts

2022-02-08

Expected to finish

2026-12-15

Last updated by the study team

2026-06-01

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects have been referred for placement of central venous access, i.e., placement of catheter, nutritional line, etc.
• Subjects with upper body venous occlusions or other conditions that preclude central venous access by conventional methods
• Subjects are willing and able to give written informed consent

You may not qualify if…

• Occlusion of the right femoral vein, right iliac vein or inferior vena cava
• Acute thrombus within any vessel to be crossed by Surfacer System (SVC, jugular, IVC, brachiocephalic and subclavian)
• Occlusion within the arterial system
• Occlusion within the coronary or cerebral vasculature

Where it is running

• Sentara Norfolk General Hospital — Norfolk, Virginia, United States (enrolling)
• Sarasota Memorial Health Care System — Sarasota, Florida, United States (enrolling)
• Emory University Hospital — Atlanta, Georgia, United States (enrolling)
• Ohio State University Hospital — Columbus, Ohio, United States (enrolling)
• Baylor Scott & White Heart and Vascular Hospital — Dallas, Texas, United States (enrolling)
• The University of Texas Health Science Center at Houston — Houston, Texas, United States (enrolling)
• St. Mark's Hospital — Millcreek, Utah, United States (enrolling)
• Pima Heart and Vascular — Tucson, Arizona, United States
• Flow Vascular Institute — Pasadena, Texas, United States

Full record on ClinicalTrials.gov

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