A Study to Obtain Additional Information on the Use of CorMatrix® CanGaroo ECM® Envelope

NCT ID: NCT02418143

Last Updated: 2023-07-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2015-09-30

Study Completion Date

2016-02-29

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Actively gather additional information on the use of CorMatrix CanGaroo ECM Envelope in a post market observational study.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Coronary Disease

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Implantable electronic device placement

CorMatrix CanGaroo ECM envelope for an implantable electronic device placement following a battery change out or upgrade.

CorMatrix CanGaroo ECM Envelope

Intervention Type DEVICE

Subjects who have received CorMatrix CanGaroo ECM Envelope for an implantable electronic device placement following a battery change or upgrade.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

CorMatrix CanGaroo ECM Envelope

Subjects who have received CorMatrix CanGaroo ECM Envelope for an implantable electronic device placement following a battery change or upgrade.

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. Subject who has received the CorMatrix CanGaroo ECM Envelope for an implantable electronic device following battery change out or upgrade.
2. Signed Informed Consent

Exclusion Criteria

1\. Known sensitivities to porcine material.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Elutia Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Director, Clinical Development

Role: STUDY_DIRECTOR

Aziyo Biologics

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

15-PR-1169

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

HemoSphere Alta Study
NCT07148323 RECRUITING
AVERT Plus Post-Market Registry
NCT02436642 TERMINATED
BIO|CONCEPT.Renamic Neo Study
NCT04350008 COMPLETED