CClinicalTrials.gg
CompletedNCT02775565Updated Dec 8, 2017

Initial Experience With the AngioVac Venous Drainage Cannula

An observational study in Heart Disease, sponsored by Angiodynamics, Inc.. Completed at 5 sites in United States. Per ClinicalTrials.gov, last updated 2017-12-08.

Sponsored by Angiodynamics, Inc. · Observational

Study type
Observational
Model
Other
Time perspective
Retrospective
Enrollment
51
Sex
All
01

Study summary

This is a retrospective, record-based study of approximately 100 patients across up to 12 centers within the United States. All patients who have been treated with the AngioVac Venous Drainage Cannula and the Extracorporeal Circuit will be considered for study participation. Eligible subject must meet all of the inclusion criteria and none of the exclusion criteria to be considered enrolled in the study. The purpose of the study is to describe initial experience with the AngioVac Venous Drainage Cannula and the Extracorporeal Circuit.

02

Conditions studied

  • Heart Disease

Browse trials for

03

In context

Heart Diseases

3,639 studies on the registry are indexed under Heart Diseases; 461 are open to participants now.

This study's enrollment of 51 is below the median of 294 across 1,241 observational studies indexed under Heart Diseases.

Browse Heart Diseases studies →

Lead sponsor

Angiodynamics, Inc. is the lead sponsor of 21 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

patients treated at each study site between February 1, 2013 and February 28, 2015 will be included.

Inclusion criteria

  • Consecutive patients treated at each study site between February 1, 2013 and February 28, 2015 will be included.

Exclusion criteria

Exclusion Criteria:

  • Patients treated with the AngioVac venous drainage system outside of those dates.
05

Study design

Observational model
Other
Time perspective
Retrospective
Enrollment
51 participants (actual)
Patient registry
No

Interventions

  • DeviceAngioVac
06

What researchers measure

Primary outcomes

  1. Detailing early clinical experience with the AngioVac Venous Drainage Cannula

    Time frame: Experience and success is determined immediately after the procedure is completed. No subject follow up data is collected and retrospective data will be reviewed.

07

Study locations

5 sites
  • Providence St. Joseph
    Burbank, California 91505, United States
  • UCLA
    Los Angeles, California 90024, United States
  • Sanford Research
    Fargo, North Dakota 58122, United States
  • MUSC
    Charleston, South Carolina 29425, United States
  • Swedish Health Services
    Seattle, Washington 98122, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 8, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02775565
Lead sponsor
Angiodynamics, Inc.
Responsible party
Sponsor
First posted
May 17, 2016
Start date
Feb 2016
Primary completion
Sep 2016
Completion
May 2017
Last update
Dec 8, 2017

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2017. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion