Curvafix® Intramedullary System for Fixation of Pelvic and Acetabular Fractures, A Post Market Evaluation

Stopped early

Conditions studied: Pelvic Ring Fracture, Acetabular Fracture, Pelvic Fracture, Pelvic Fracture Acetabulum

In brief

Prospective, single arm, post-market evaluation to evaluate the use and performance of the IM Implant in a post market setting.

Key facts

Study ID

NCT05606042

Run by

CurvaFix, Inc.

People needed

53

Starts

2021-11-24

Expected to finish

2023-03-09

Last updated by the study team

2026-03-20

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subject, or their Authorized Representative, is willing and able to provide written informed consent, including authorization to release health information
• Subject has undergone pelvic or acetabular fixation using the IM Implant and the IM Implant was placed according to the manufacturer's labeling.
• Subject's pelvic or acetabular fixation with the IM Implant occurred within the last 30 calendar days.

You may not qualify if…

• Subject is unwilling or unable to provide written informed consent and/or does not have an authorized representative who can provide consent on their behalf
• Subject presents with any condition or situation which, in the Investigator's opinion, puts the Subject at risk, could confound the study results, or may interfere with the Subject's participation in the study

Where it is running

• Memorial Medical Center, Springfield — Springfield, Illinois, United States
• Missouri Orthopaedic Institute — Columbia, Missouri, United States
• Mount Carmel Research Institute — Columbus, Ohio, United States
• University of Pennsylvania, Perelman School of Medicine — Philadelphia, Pennsylvania, United States
• Prisma Health — Columbia, South Carolina, United States
• UT Health San Antonio — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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