Clinical Trials Directory

Trials / Completed

CompletedNCT04090320

CATERPILLAR™ Arterial Embolization Device Study

A Prospective, Multi-Center, Single-Arm Study Assessing the Clinical Use of the CATERPILLAR™ Arterial Embolization Device System for Arterial Embolization in the Peripheral Vasculature (CHRYSALIS)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
C. R. Bard · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The primary objective of this study is to evaluate the performance and safety of the CATERPILLAR™ Arterial Embolization Device when used for arterial embolization in the peripheral vasculature.

Detailed description

This feasibility study is a prospective, multi-center, single-arm study of the CATERPILLAR™ Arterial Embolization Device. Up to twenty (20) subjects will be treated with the CATERPILLAR™ Arterial Embolization Device at up to 5 investigational sites in New Zealand and Australia.

Conditions

Interventions

TypeNameDescription
DEVICECATERPILLAR™ Arterial Embolization DevicePlacement of the CATERPILLAR™ Arterial Embolization Device for patients requiring arterial embolization in the peripheral vasculature.

Timeline

Start date
2019-09-25
Primary completion
2020-11-04
Completion
2020-11-04
First posted
2019-09-16
Last updated
2021-01-15

Locations

5 sites across 2 countries: Australia, New Zealand

Source: ClinicalTrials.gov record NCT04090320. Inclusion in this directory is not an endorsement.