Comparative Evaluation of Minimally Invasive "Tibial Tuberoplasty" Surgical Technique Versus Conventional Open Surgery for Tibial Plateau Fractures (TUBERIMPACT)
Schatzker Type 2 or 3 Tibial Plateau Fracture
About this trial
This is an interventional treatment trial for Schatzker Type 2 or 3 Tibial Plateau Fracture focused on measuring tibial plateau fracture, minimally invasive surgery, ballon reduction
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 18 years old.
- Patients with a Schatzker type 2 or 3 tibial plateau fracture (compression with or without split) demonstrated on CT-scan and located in the lateral or medial condyle of tibia.
- Patients with fractures caused by trauma.
- Patients with fractures 10 days old maximum.
- Understand and accept the constraints of the study.
- Be a beneficiary or affiliated member of a Health Insurance plan.
- Give written consent for the study after having received clear information.
Exclusion Criteria:
- Age < 18 years old.
- Patients with fractures resulting from osteolysis.
- Patients with open fractures.
- Patients with fractures more than 10 days old.
- Patients with concomitant fracture(s) or condition(s) during the trauma reducing the range of motion.
- Patients unable to walk before the injury.
- History of sepsis in the injured knee.
- Contraindications to anesthesia, contrast agent, medical devices or cement.
- History of hypersensitivity reactions to contrast media, bone filler or metal.
- Patients with a degenerative joint disease (polyarthritis, etc.).
- Absence of signature of the informed consent form.
- Patients not covered by French national health insurance.
- Subjects requiring closer protection, i.e. minors, pregnant women, nursing mothers, subjects deprived of their freedom by a court or administrative decision, subjects admitted to a health or social welfare establishment, major subjects under legal protection, and finally patients in an emergency setting.
Sites / Locations
- CHU d'Amiens
- CHU Angers
- AP-HP / Hopital Ambroise Paré
- CHU de Brest
- CHU Dijon
- CHU de Nantes
- CHU de Poitiers
- CHU de Rennes
- CHU Rouen
- CHRU Tours
- CH Versailles
- CHU de Martinique
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Control group
Experimental group
The patients will be treated with an open technique: cutaneous incision with submeniscal arthrotomy under guidance of a fluoroscope. The reduction will be performed using a spatula, a bone tamp or open reduction internal fixation. The osteosynthesis and filling of the cavity will be performed by the same surgical access.
The patients will be treated with the "Tibial Tuberoplasty" technique under fluoroscopic guidance with or without arthroscopy. The reduction will be performed by an anterior approach using a kyphoplasty balloon. The combined osteosynthesis including cannulated screws and cementoplasty will both be performed by a percutaneous technique.