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Lisfranc Fracture
Clinical trial pipeline · Data from ClinicalTrials.gov
See which Lisfranc Fracture trials you may qualify forClinical trial pipeline · Data from ClinicalTrials.gov
See which Lisfranc Fracture trials you may qualify forThe study in question is a post market clinical follow up (PMCF) study to evaluate the safety and performance of bioabsorbable headless compression screw Inion…
The objective of the registry is to evaluate the continued safety and performance of Arthrex foot and ankle products, including the ProStop® implant for hyperpr…
Analgesic drug study that will compare pain outcomes of opioid analgesia and opioid-free analgesia in post-operative orthopedic patients.
This study is a multicenter prospective randomized control trial comparing hardware retention (HR) to removal of hardware (RH).
The aim of the proposed study is to define the optimal treatment for Lisfranc fracture-dislocation, either primary arthrodesis (PA) or open reduction and intern…
I hypothesize that absorbable screw fixation of the foot's Lisfranc ligaments does not yield significant differences in postoperative foot stability, ligament f…