Actively Recruiting
Weight-bearing of Patients After Pelvic Ring Fracture
Led by University Hospital, Grenoble · Updated on 2024-07-01
250
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
CONDITIONS
Official Title
Weight-bearing of Patients After Pelvic Ring Fracture
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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.
You will not qualify if you...
- Ipsi-lateral fracture of the femoral and/or associated acetabulum (Floating Hip C or B)
- Pregnant and breastfeeding women
- People under guardianship, protected adults
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Grenoble Alpes university Hospital,La tronche
Grenoble, France
Actively Recruiting
Research Team
M
Mehdi PI BOUDISSA, Pr
CONTACT
S
Sarah KASSAR-UNEISI
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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