RECRUITING

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

Description

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

Conditions

Pelvic Ring FractureAcetabular FracturePelvic FracturePelvic Fracture Acetabulum
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Related Conditions:

Pelvic Ring FractureAcetabular FracturePelvic FracturePelvic Fracture Acetabulum

Study Overview

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Study Details

Study overview

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

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

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

Condition
Pelvic Ring Fracture
Intervention / Treatment

-

Contacts and Locations

Springfield

Memorial Medical Center, Springfield, Springfield, Illinois, United States, 62781

Columbia

Missouri Orthopaedic Institute, Columbia, Missouri, United States, 65212

Columbus

Mount Carmel Research Institute, Columbus, Ohio, United States, 43219

San Antonio

UT Health San Antonio, San Antonio, Texas, United States, 78229

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * 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.
  • * 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

Ages Eligible for Study

to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

CurvaFix, Inc.,

Jennifer Hebert, STUDY_DIRECTOR, Clin-Assist, LLC

Study Record Dates

2024-06