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Initial Experience With the AngioVac Venous Drainage Cannula - Trial NCT02775565

Access comprehensive clinical trial information for NCT02775565 through Pure Global AI's free database. This phase not specified trial is sponsored by Angiodynamics, Inc. and is currently Completed. The study focuses on Heart Disease. Target enrollment is 51 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT02775565
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Trial Details
ClinicalTrials.gov โ€ข NCT02775565
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Initial Experience With the AngioVac Venous Drainage Cannula
Initial Experience With the AngioVac Venous Drainage Cannula and Cardiopulmonary Bypass Circuit: A Retrospective, Multi-Center Chart Review

Study Focus

Heart Disease

AngioVac

Observational

device

Sponsor & Location

Angiodynamics, Inc.

Burbank,Los Angeles,Fargo,Charleston,Seattle, United States of America

Timeline & Enrollment

N/A

Feb 01, 2016

May 01, 2017

51 participants

Primary Outcome

Detailing early clinical experience with the AngioVac Venous Drainage Cannula

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.

ICD-10 Classifications

Heart disease, unspecified
Complications and ill-defined descriptions of heart disease
Other ill-defined heart diseases
Other forms of heart disease
Hypertensive heart disease

Data Source

ClinicalTrials.gov

NCT02775565

Device Trial