Coronary Artery Disease Clinical Trial
— SECUREOfficial title:
Sternal Rigid Fixation: Evaluation of Clinical Outcomes Using Real-World Evidence
NCT number | NCT03709693 |
Other study ID # | 0518 |
Secondary ID | |
Status | Terminated |
Phase | |
First received | |
Last updated | |
Start date | May 14, 2019 |
Est. completion date | May 13, 2020 |
Verified date | July 2021 |
Source | Zimmer Biomet |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
The primary objective of this study is to evaluate the rate of deep sternal wound infection at 30 days post-operative following a full median sternotomy in patients treated with SternaLock Blu for rigid sternal fixation. This study will also provide evidence of the clinical performance of SternaLock Blu for up to 90 days using real world evidence methodology. Sternal complications will be reported through 90 days follow up.
Status | Terminated |
Enrollment | 156 |
Est. completion date | May 13, 2020 |
Est. primary completion date | May 13, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 100 Years |
Eligibility | Inclusion Criteria: 1. = 18 years of age, no upper limit 2. Undergoing a full standard midline sternotomy as part of an elective or urgent cardiac surgical procedure [i.e., coronary artery bypass graft (CABG) and/ or valve replacement along with other cardiac surgical procedures] and closed with the SternaLock Blu Sternal Closure System 3. Willing and able to return for follow-up Exclusion Criteria: Preoperative 4. Emergent or salvage cardiac acuity i.e., patients undergoing cardiopulmonary resuscitation en-route to the operating room or prior to induction of anesthesia 5. Any contraindication listed in the SternaLock Blu instructions for use (IFU/ Appendix 3) (active infection, foreign body sensitivity, or mental/ neurologic conditions who are unwilling or incapable of following post-operative care instructions) Operative 6. Delayed sternal closure required for any reason 7. Intra-operative conditions that, in the opinion of the operating surgeon, would preclude the use of rigid plate fixation, i.e.: insufficient quantity of sternal bone or compressible sternum indicating poor bone quality, as assessed by the operating surgeon using his or her professional judgment at the time of closure 8. Use of bone wax between the sternal halves 9. Intraoperative death prior to device placement |
Country | Name | City | State |
---|---|---|---|
United States | University of Virginia | Charlottesville | Virginia |
United States | St. Franciscan Health | Indianapolis | Indiana |
United States | Saint Luke's Hospital of Kansas City | Kansas City | Missouri |
United States | Cardiovascular Surgery Clinic, PLLC | Memphis | Tennessee |
Lead Sponsor | Collaborator |
---|---|
Zimmer Biomet |
United States,
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CCS
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NYHA
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* Note: There are 42 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Deep Sternal Wound Infection Rate | DSWI is defined as deep infection involving muscle, bone, and/ or mediastinum requiring operative intervention and has all of the following conditions:
Wound opened with excision of tissue (I&D) or re-exploration of mediastinum Positive culture unless patient on antibiotics at the time of culture or no culture obtained Treatment with antibiotics beyond perioperative prophylaxis |
at 30 days post operatively up to 90 days |
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