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Weight-bearing of Patients After Pelvic Ring Fracture

Weight-bearing of Patients After Pelvic Ring Fracture: A Monocentric Observational Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06481865
Acronym
RECFAP
Enrollment
250
Registered
2024-07-01
Start date
2024-06-01
Completion date
2025-06-01
Last updated
2024-07-01

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

Conditions

Weight-bearing of Patients After Pelvic Ring Fracture

Brief summary

Pelvic ring fractures are fractures associated with high morbidity and mortality. When the fracture is displaced, surgical management to achieve reduction and fixation of the anterior and posterior annulus is the current reference. The optimal technique that gives the best results is controversial. Open reductions and internal fixations (ORIFs) are associated with more blood loss and a higher rate of infection, while closed reductions and percutaneous fixations (CRPF) are associated with more screw misplacements and thus vascular or nerve damage. The results appear to be similar in the literature between the two approaches Surgery for pelvic ring fractures has become increasingly common over the past three decades Recovery is often delayed for weeks post-surgery, depending on the center. Modern management emphasizes early rehabilitation, including early mobility and weight-bearing, when possible. Increasing the number of screws, their diameter and length, and systematically fixing both anterior and posterior lesions add safety for early reloading The aim of the study is The main objective of the study is to evaluate the clinical outcome associated with early weight-bearing in patients operated on for a pelvic ring fracture in a large cohort of patients at Grenoble University Hospital, compared to patients operated on for the same type of pelvic ring fracture with delayed weight-bearing. The investigator hypothesize that early weight-bearing of pelvic ring fractures with biomechanically stable fixation does not result in significant differences in clinical outcomes at a minimum of one year compared to patients with delayed weight-bearing

Interventions

None listed

Sponsors

University Hospital, Grenoble
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Adult patient at the time of injury * Pelvic ring fracture * Pre-operative X-rays * Pre-operative CT scan * Post-operative X-rays * Postoperative CT scan * Willingness and ability to participate in the study.

Exclusion criteria

* Ipsi-lateral fracture of the femoral and/or associated acetabulum (Floating Hip C or B) * Pregnant and breastfeeding women * People under guardianship, protected adults

Design outcomes

Primary

MeasureTime frameDescription
Evaluate the clinical outcome associated with early weight-bearing in patients operated on for a pelvic ring fracture compared to patients operated on for the same type of pelvic ring fracture with delayed weight-bearing1 yearClinical outcomes according to functional assessment ( Majeed score)

Secondary

MeasureTime frameDescription
Define the prognostic factors associated with poor clinical outcomes and Pseudoarthrosis or vicious callus.1 yearPrognostic factors from operative data (Ilio-inguinale,Ilio-stoppa,stoppa,stoppa + external window,kocher-Langenbeck, anterior + posterior, operating time (min), blood loss (ml),intraoperative re-transfusion (ml))
Compare clinical outcomes and radiological results with the literature1 yearClinical outcomes according to functional assessment (MAJEED score)
Evaluation of the outcomes and complications of immediate weight-bearing in elderly patients.1 yearIntraoperative and postoperative complications (including complications of immediate weight-bearing)

Countries

France

Contacts

Primary ContactMehdi PI BOUDISSA, Pr
MBoudissa@chu-grenoble.fr0476769693
Backup ContactSarah KASSAR-UNEISI
SUneisi@chu-grenoble.fr0033476767524

Outcome results

None listed

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