New curved rod shows promise for tough pelvic breaks
NCT ID NCT05606042
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a special curved rod implant designed to fix broken pelvic and hip socket bones. It included 53 adults who had already received the implant. Researchers tracked whether patients needed more surgeries and how well they could move and bear weight afterward.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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53 people
The number who actually took part.
- Started
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Nov 2021
- Finished
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Mar 2023
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Participants will be selected from medical facility study sites that have agreed to participate in the study.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion 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. Exclusion Criteria: * 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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Memorial Medical Center, Springfield
Springfield, Illinois, 62781, United States
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Missouri Orthopaedic Institute
Columbia, Missouri, 65212, United States
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Mount Carmel Research Institute
Columbus, Ohio, 43219, United States
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Prisma Health
Columbia, South Carolina, 29203, United States
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UT Health San Antonio
San Antonio, Texas, 78229, United States
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University of Pennsylvania, Perelman School of Medicine
Philadelphia, Pennsylvania, 19104, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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