Condition: Hyperpronated Foot · Reconstruction Surgeries of the Foot · Fixation of Fractures and Fusion (Bunionectomy Osteotomies) of the Foot/Ankle · Sponsor: Arthrex, Inc.
The objective of the registry is to evaluate the continued safety and performance of Arthrex foot and ankle products, including the ProStop® implant for hyperpronated foot; Bio-Compression Screw for reconstruction surgeries of the foot; TRIM-IT Drill Pin® system and/or TRIM-IT Spin Pin™ system for fixation of fractures and fusion (bunionectomy osteotomies) of the foot/ankle; Headless Compression Screws and Compression FT Screws for fixation of small bone fragments of the foot/ankle; DynaNite® nitinol staple for midfoot and hindfoot arthrodeses or osteotomies, first metatarsophalangeal arthrodesis, and mono or bi-cortical osteotomies in the forefoot; BioComposite SutureTak® anchor for medial ankle stabilization; Beveled FT Screws for hallux valgus repair; KreuLock™ screws for ankle fractures; ArthroFLEX® dermal allograft for hallux rigidus arthroplasty; and DualCompression Hindfoot Nail for tibiotalocalcaneal arthrodesis.
This description comes directly from the study's public registry record.
Justin Moss, DHSc · 770 584 4972 · justin.moss@arthrex.com
Always discuss trial participation with your own doctor first.
| UC Davis Medical Center | Sacramento, California, United States | Recruiting |
| Northwestern University | Chicago, Illinois, United States | Recruiting |
| TOA Research Foundation | Nashville, Tennessee, United States | Terminated |
| Barrett Podiatry | San Antonio, Texas, United States | Terminated |
| Atlantic Orthopaedic Specialists | Virginia Beach, Virginia, United States | Recruiting |
| OrthoPedes | Duisburg, Germany | Terminated |
| Dr Haroun Mahomed Orthopaedic Practice | Durban, South Africa | Terminated |
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Source record: clinicaltrials.gov/study/NCT04715139