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Sternal Rigid Fixation: Evaluation of Clinical Outcomes Using Real-World Evidence
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.
The primary endpoint for this study is the rate of deep sternal wound infection (DSWI) at 30 days post-operative, following a midline sternotomy closed with SternaLock Blu. DSWI is defined as deep infection involving muscle, bone, and/ or mediastinum requiring operative intervention and has all of the following conditions: 1. Wound opened with excision of tissue or re-exploration of mediastinum 2. Positive culture unless patient on antibiotics at the time of culture or no culture obtained 3. Treatment with antibiotics beyond perioperative prophylaxis Post-operative sternal wound complications occurring within 90 days post-operative. Outcomes will be reported up to 90 days after surgery, including data on adverse events associated with the use of SternaLock Blu Sternal Closure System from the moment of implantation to the end-of-study.
Age
18 - 100 years
Sex
ALL
Healthy Volunteers
Yes
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, United States
University of Virginia
Charlottesville, Virginia, United States
Start Date
May 14, 2019
Primary Completion Date
May 13, 2020
Completion Date
May 13, 2020
Last Updated
July 23, 2021
156
ACTUAL participants
SternaLock Blu
DEVICE
Lead Sponsor
Zimmer Biomet
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05208567