Fragility Fractures of the Pelvis (FFP)

Running, not enrolling

Conditions studied: Pelvic Fracture

In brief

Prospective data will be collected in approximately 420 patients, above the age of 65, suffering from an FFP type fracture equal to or higher than type II, according to Rommens and Hofmann. Patients will be followed up according to the standard (routine) for up to 1 year after the treatment. Data collection will include underlying disease, treatment details, functional and patient reported outcomes (PRO)s, radiological outcomes, and anticipated or procedure-related adverse events (i.e. complications).

Key facts

Study ID

NCT04182776

Run by

AO Innovation Translation Center

People needed

420

Starts

2022-03-01

Expected to finish

2027-07-01

Last updated by the study team

2026-07-13

Who can join

Age: 65 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age 65 years or older at time of injury
• Diagnosis, via CT scan as per standard of care, of FFP grade II or higher according to the Rommens and Hofmann classification (including fractures of the anterior pelvic ring involving the anterior lip of the acetabulum not regarded as the acetabular fractures)
• Informed consent obtained, ie:
• Ability to understand the content of the patient information/ICF
• Willingness and ability to participate in the registry according to the standard of care in each clinic
• Signed and dated Ethics Committee (EC)/ Institutional Review Board (IRB) approved written informed consent OR
• Written consent provided according to the IRB/EC defined and approved procedures for patients who are not able to provide independent written informed consent

You may not qualify if…

• Pelvic fractures that do not meet the criteria of a fragility fracture (ie, high-energy trauma)
• FFP type I fractures
• Concomitant fractures of the acetabulum (except anterior lip of the acetabulum, see above)
• Pathological fractures (ie, patients with malignant or metastatic diseases of the pelvis, infections)
• Concomitant osteoporotic fractures outside of pelvis
• Participation in any other medical device or medicinal product study within the previous month that could influence in opinion of the PI the results of the present registry

Where it is running

• University of Missouri — Columbia, Missouri, United States
• The Ottawa Hospital - Civic Campus — Ottawa, Canada
• University Medical Center Hamburg Eppendorf — Hamburg, Germany
• University Hospital Leipzig — Leipzig, Germany
• University Medical Center Johannes Gutenberg-University — Mainz, Germany
• Queen Mary Hospital — Hong Kong, Hong Kong
• Okayama medical hospital — Okayama, Japan
• University Medical Center Groningen — Groningen, Netherlands
• Radboud University Medical Center — Nijmegen, Netherlands
• Cantonal Hospital Lucerne — Lucerne, Switzerland

Full record on ClinicalTrials.gov

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