NCT06481865 Weight-bearing of Patients After Pelvic Ring Fracture
| NCT ID | NCT06481865 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University Hospital, Grenoble |
| Condition | Weight-bearing of Patients After Pelvic Ring Fracture |
| Study Type | OBSERVATIONAL |
| Enrollment | 250 participants |
| Start Date | 2024-06-01 |
| Primary Completion | 2025-06-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 250 participants in total. It began in 2024-06-01 with a primary completion date of 2025-06-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
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
Eligibility Criteria
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
Contact & Investigator
Mehdi PI BOUDISSA
PRINCIPAL INVESTIGATOR
Grenoble Alpes University Hospital
Frequently Asked Questions
Who can join the NCT06481865 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 100 Years, studying Weight-bearing of Patients After Pelvic Ring Fracture. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06481865 currently recruiting?
Yes, NCT06481865 is actively recruiting participants. Contact the research team at MBoudissa@chu-grenoble.fr for enrollment information.
Where is the NCT06481865 trial being conducted?
This trial is being conducted at Grenoble, France.
Who is sponsoring the NCT06481865 clinical trial?
NCT06481865 is sponsored by University Hospital, Grenoble. The principal investigator is Mehdi PI BOUDISSA at Grenoble Alpes University Hospital. The trial plans to enroll 250 participants.