An Observational Study of Radial Access Embolization Procedures Using HydroPearl Microspheres

Completed

Conditions studied: Uterine Fibroid, Arteriovenous Malformations, Hypervascular Tumors, Benign Prostatic Hyperplasia

In brief

This registry study is designed to collect data on the procedural success and complication rates in real-world patients undergoing HydroPearl embolization procedures via radial access.

Key facts

Study ID

NCT04272216

Run by

Terumo Medical Corporation

People needed

99

Starts

2020-02-06

Expected to finish

2023-03-11

Last updated by the study team

2025-09-09

Who can join

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

You may qualify if…

• Subject is ≥ 18 years old
• Subject is scheduled for a procedure for treatment with HydroPearl microspheres using radial access.
• Subject is willing and able to complete follow-up requirements
• Subject is willing and able to sign a written Informed Consent form prior to participating in the registry.

You may not qualify if…

• Unable to have a procedure with radial access for any reason.
• Participating in another clinical study which, in the opinion of the investigator, could impact the results of this registry.
• Pregnant or planning to become pregnant during the study.

Where it is running

• University of California - Los Angeles — Los Angeles, California, United States
• Rush University Medical Center — Chicago, Illinois, United States
• SLU Department of Radiology — St Louis, Missouri, United States
• Mount Sinai — New York, New York, United States
• UNC — Chapel Hill, North Carolina, United States
• Medical University of South Carolina — Charleston, South Carolina, United States

Full record on ClinicalTrials.gov

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