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Surgical Treatment of Pelvis in Fragility Fracture in Germany: a Prospective, National, Multicenter, Observational, Comparative Cohort Study Comparing Isolated Posterior Versus Combined Anterior-posterior Surgical Fracture Stabilization

Surgical Treatment of Pelvis in Fragility Fracture in Germany: a Prospective, National, Multicenter, Observational, Comparative Cohort Study Comparing Isolated Posterior Versus Combined Anterior-posterior Surgical Fracture Stabilization

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06550934
Acronym
AO TOP
Enrollment
420
Registered
2024-08-13
Start date
2025-03-31
Completion date
2027-10-31
Last updated
2025-02-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pelvis; Fracture

Keywords

Pelvis, Fragility fracture, Classification, Management, Operative, Outcome

Brief summary

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.

Interventions

PROCEDUREFracture stabilization

isolated posterior surgical fracture stabilization vs. combined anterior-posterior surgical fracture stabilization

Sponsors

AUC - Akademie der Unfallchirurgie
CollaboratorUNKNOWN
AO Trauma Deutschland e.V.
CollaboratorOTHER
AO Innovation Translation Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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. * Low-energy trauma fracture, or osteoporotic fracture, or insufficiency fracture, or spontaneous fracture * ASA-Score ≤ 3 pts. * Ability to provide informed consent according to the IRB/EC defined and approved procedures

Exclusion criteria

* 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) * History of pelvic fracture or pelvic ring surgery (hip joint implants do not count) * Clinically significant or unstable medical or surgical condition that prevents surgical treatment

Design outcomes

Primary

MeasureTime frameDescription
Pain ratingNumeric Rating Scale (NRS) 3 month after surgical fixation of the fragility fracture of the pelvisPerception of pain will be assessed using Numeric Rating Scale (NRS) from 1-10, where patient reports pain due to his/her pelvis fracture. A higher value correlates with greater pain.

Contacts

Primary ContactCynthia Sob, PhD
cynthia.sob@aofoundation.org+41798937428

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026