Actively Recruiting
US Post-Market Surveillance Study of the Surfacer System
Led by Merit Medical Systems, Inc. · Updated on 2025-08-05
30
Participants Needed
6
Research Sites
253 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
US Post-Market Surveillance Study of the Surfacer System
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Referred for placement of central venous access such as catheter or nutritional line
- Have upper body venous occlusions or conditions that prevent central venous access by conventional methods
- Willing and able to give written informed consent
You will not qualify if you...
- Occlusion of the right femoral vein, right iliac vein, or inferior vena cava
- Acute thrombus in any vessel to be crossed by the Surfacer System (SVC, jugular, IVC, brachiocephalic, subclavian)
- Occlusion within the arterial system
- Occlusion within the coronary or cerebral vasculature
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 6 locations
1
Pima Heart and Vascular
Tucson, Arizona, United States, 85704
Completed
2
Sarasota Memorial Health Care System
Sarasota, Florida, United States, 34239
Actively Recruiting
3
Baylor Scott & White Heart and Vascular Hospital
Dallas, Texas, United States, 75226
Actively Recruiting
4
The University of Texas Health Science Center at Houston
Houston, Texas, United States, 77030
Actively Recruiting
5
Flow Vascular Institute
Pasadena, Texas, United States, 77504
Completed
6
St. Mark's Hospital
Millcreek, Utah, United States, 84124
Actively Recruiting
Research Team
H
Hannah Susmeyer
CONTACT
V
Vicky Brunk, RN
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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