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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04351269
Other study ID # CPR-2212
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 22, 2020
Est. completion date June 30, 2021

Study information

Verified date July 2023
Source Aziyo Biologics, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The objective of this study is to retrospectively gather information on patients who underwent a CIED procedure with either a CanGaroo Envelope, TYRX Envelope, or no envelope.


Description:

A single center will retrospectively review up to 700 subjects who underwent implantation of a CIED with a CanGaroo Envelope, TYRX Envelope, or no envelope. All sets of subjects enrolled will also be examined for any follow-up visits and/or adverse events that occurred up to 12 months post-surgery.


Recruitment information / eligibility

Status Completed
Enrollment 597
Est. completion date June 30, 2021
Est. primary completion date June 30, 2021
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Any patient that had a CIED implanted with either a CanGaroo Envelope, a TYRX Envelope, or no envelope on or after March 27, 2017 Exclusion Criteria: - Any patient that had a CIED implanted with any other type of envelope - Any patient that had a CIED implanted prior to March 27, 2017

Study Design


Intervention

Device:
CanGaroo Envelope
CanGaroo Envelope with Cardiac Implantable Electronic Device (CIED) implantation
TYRX Envelope
TYRX Envelope with Cardiac Implantable Electronic Device (CIED) implantation

Locations

Country Name City State
United States Piedmont Athens Electrophysiology Athens Georgia

Sponsors (1)

Lead Sponsor Collaborator
Aziyo Biologics, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Participants With Major Infection Post Procedure Major CIED infections are defined as a CIED infection resulting in one or more of the following:
CIED system removal
Any invasive procedure (e.g., pocket opened) without system removal
Treatment with antibiotic therapy if the subject is not a candidate for system removal and infection recurrence after completion of antibiotic therapy or evidence of deep infection with wound dehiscence, erosion, or purulent drainage
Death
12 months post procedure
Secondary Number of Participants With Pocket Related Issues Prompting an Office Visit Any pocket related issues that prompted an office visit 12 months post procedure
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