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

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

Status

Withdrawn

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02418143

Acronym

JUMP

Enrollment

Registered

2015-04-16

Start date

2015-09-30

Completion date

2016-02-29

Last updated

2023-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Disease

Brief summary

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

Interventions

DEVICECorMatrix CanGaroo ECM Envelope

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

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

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.

Design outcomes

Primary

Measure	Time frame
Device Related Adverse Events	1 day post-operative follow up visit

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026