Evaluate the Continued Safety and Performance of the Foot and Ankle Products
Public ClinicalTrials.gov record NCT04715139. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Multi-Center, Prospective Registry to Evaluate the Continued Safety and Performance of the Foot and Ankle Products
Study identification
- NCT ID
- NCT04715139
- Recruitment status
- Recruiting
- Study type
- Observational
- Phase
- Not listed
- Lead sponsor
- Arthrex, Inc.
- Industry
- Enrollment
- 700 participants
Conditions and interventions
Conditions
- Akin Osteotomy
- Arthrodesis of the Metatarsocuneiform Joint to Reposition and Stabilize Metatarsus Primus Varus
- First Metatarsophalangeal Arthrodesis
- Fixation of Fractures and Fusion (Bunionectomy Osteotomies) of the Foot/Ankle
- Fixation of Osteotomies for Hallux Valgus Treatment (Scarf and Chevron)
- Fixation of Small Bone Fragments of the Foot/Ankle
- Hyperpronated Foot
- Lisfranc Arthrodesis
- Medial Ankle Stabilization
- Midfoot and Hindfoot Arthrodeses or Osteotomies
- Mono or Bi-cortical Osteotomies in the Forefoot
- Osteotomy Fixation of Hallux Valgus Repair (Such as Scarf and Chevron Etc.)
- Reconstruction Surgeries of the Foot
- Tibiotalocalcaneal Arthrodesis
Interventions
- Products listed in Group/Cohort Description Device
Device
Eligibility (public fields only)
- Age range
- 2 Years and older
- Sex
- All
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Nov 30, 2020
- Primary completion
- Nov 30, 2027
- Completion
- Dec 30, 2027
- Last update posted
- Feb 10, 2026
2020 – 2027
United States locations
- U.S. sites
- 5
- U.S. states
- 5
- U.S. cities
- 5
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| UC Davis Medical Center | Sacramento | California | 95817 | Recruiting |
| Northwestern University | Chicago | Illinois | 60611 | Recruiting |
| TOA Research Foundation | Nashville | Tennessee | 37209 | Terminated |
| Barrett Podiatry | San Antonio | Texas | 78258 | Terminated |
| Atlantic Orthopaedic Specialists | Virginia Beach | Virginia | 23462 | Recruiting |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
Non-U.S. locations
This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT04715139, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Feb 10, 2026 · Synced May 20, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT04715139 live on ClinicalTrials.gov.