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Completed No phase listed Observational

Comparison of Participants Who Received a CanGaroo® Envelope, TYRX™ Envelope, or no Envelope During CIED Implantation

ClinicalTrials.gov ID: NCT04645173

Public ClinicalTrials.gov record NCT04645173. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 1:48 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-Center Study Evaluating Participants Who Received CanGaroo® Envelope, TYRX™ Envelope, or No Envelope During CIED Implantation

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of this study is to gather information on participants returning at time of CIED change-out or revision who underwent a device implantation with either a CanGaroo® envelope, TYRX™ envelope, or no envelope.

Study identification

NCT ID
NCT04645173
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Elutia Inc.
Industry
Enrollment
46 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 1, 2021
Primary completion
Oct 30, 2023
Completion
Dec 30, 2023
Last update posted
Jan 8, 2024

2021 – 2023

United States locations

U.S. sites
11
U.S. states
8
U.S. cities
10
Facility City State ZIP Site status
Valley Heart Rhythm Specialists Chandler Arizona 85224
Bay Pines VA Bay Pines Florida 33744
Baptist Medical Center Jacksonville Florida 32207
University of Florida Jacksonville Florida 32209
Prairie Education & Research Cooperative / St. John's Hospital Springfield Illinois 62769
U of L Health/Jewish Hospital Louisville Kentucky 40241
Columbia University Irving Medical Center New York New York 10032
Atrium Health Concord North Carolina 28025
East Carolina University/Vidant Medical Center Greenville North Carolina 27834
Penn Presbyterian Medical Center Philadelphia Pennsylvania 19104
University of Virginia Medical Center Charlottesville Virginia 22903

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04645173, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 8, 2024 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04645173 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →