Zimmer Biomet-RibFix Titan

Part of paid clinical trials in Indianapolis, Indiana.

Sponsor
Zimmer Biomet
Study ID
NCT07485829
Status
Recruiting
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Conditions

  • Rib Fracture
  • Rib Fracture Multiple

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • The RibFix Titan™ device should be used within this arm of the study. — DEVICE
    Rib Fixation

Study Details

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.

Key Dates

Start date
Mar 31, 2026
Status verified
Apr 2026
Primary completion
Jul 31, 2027
Completion
Mar 31, 2028

Study Design

Enrollment
54 participants (estimated)

Arms

  • Arm: Rib Fixation
    Consecutive patients will undergo rib fixation procedure using the RibFix Titan fixation system.

Primary Outcome Measure

Evaluation of Patient Safety [ Time Frame: 90 days ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Ascension St. Vincent HospitalIndianapolisIndiana46260
Jamie Williams
[email protected]
317-210-3487
Nakul Valsangkar, MD (PRINCIPAL_INVESTIGATOR)
Lewis Jacobson, MD (SUB_INVESTIGATOR)

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By research site
Ascension St. Vincent Hospital· Indianapolis, IN

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