About this trial
Over a period of approximately two years, patients above the age of 65 who have suffered from an FFP equal to or higher than type IIc FFP, according to Rommens and Hofmann, will be eligible for inclusion. At least 420 patients will be included and followed up up for 12 months. Treatment and postoperative care, will be as per standard of care at the participating institution, with a free choice of isolated posterior or combined anterior-posterior surgical treatment.
Pain levels, quality of life, level of mobility and independence will be assessed at different time points. Furthermore, both clinical and radiographic outcomes, complications, morbidity and mortality associated with interventions will be evaluated. Assessment and evaluation will be performed at defined time points during FU according to standard of care.
Eligibility criteria
Qualifiers
Patients with sacral FFP (no concomitant injuries) Types: IIc, IIIc, IVb, IVc according to Rommens and Hofmann associated with fracture of the anterior pelvic ring (fractures involving the anterior lip of the acetabulum that are not regarded as acetabular fracture will be included)
Diagnostic workup for fracture diagnosis and classification performed using CT scan as per standard of care
Indication for surgical fracture fixation as considered by the attending surgeon
Age ≥ 65 yrs.
Disqualifiers
Patients with multiple fractures
Instability of the pubic symphysis (ie, visibility of a widening or diastasis of the symphysis), and/or fractures of the pubic rami next to the symphysis, that indicate instability
Pelvic fractures due to high-energy trauma
Pathologic fractures (eg, fractures caused by malignancy or infection)
Trial design
Treatments tested in this trial
- Fracture stabilization
Treatment groups
Locations
Sponsors and collaborators
AO Innovation Translation Center
Lead sponsor
AUC - Akademie der Unfallchirurgie
Collaborator
AO Trauma Deutschland e.V.
Collaborator