Actively Recruiting
Zimmer Biomet-RibFix Titan
Led by Zimmer Biomet · Updated on 2026-04-21
54
Participants Needed
1
Research Sites
100 weeks
Total Duration
On this page
Sponsors
Z
Zimmer Biomet
Lead Sponsor
R
Riverpoint Medical
Collaborating Sponsor
AI-Summary
What this Trial Is About
Prospective, single-center, non-randomized, single-cohort, post-market clinical follow-up study to confirm the safety, performance, and clinical benefits for the use of the RibFix Titan™ system implants and instrumentation) in the fusion, stabilization, and fixation of fractures in the chest wall including rib reconstructive surgical procedures, trauma, or planned osteotomies.
CONDITIONS
Official Title
Zimmer Biomet-RibFix Titan
Who Can Participate
Eligibility Criteria
You may qualify if you...
- At least 18 years of age
- Willing and able to sign an Institutional Review Board (IRB) approved Informed Consent Form and able to comply with study requirements, in the Investigator's opinion
- Independent of study participation, patient qualifies for fixation, stabilization, and/or fusion of rib fractures or osteotomies of normal and osteoporotic bone with the study device
You will not qualify if you...
- Midline Sternotomy: sternotomy incisions crossing the midline
- Active Infection: patients should not have any ongoing infections
- Material Sensitivity: where sensitivity to materials is suspected, comprehensive testing should be conducted before implantation
- Inability to Adhere to Post-operative Care: Patients must have the ability and willingness to comply with post-operative care instructions, which may not be possible for individuals with certain mental or neurological conditions
- Patients not expected to survive the duration of follow-up due to the involvement of trauma situations
- Patients with a history of alcohol or substance abuse, as well as vulnerable populations such as prisoners and pregnant women
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Ascension St. Vincent Hospital
Indianapolis, Indiana, United States, 46260
Actively Recruiting
Research Team
M
Megan McKinnie
CONTACT
L
Lynsey Boyle
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here