Safety and Performance of PEEK Anchors in Extremities
Public ClinicalTrials.gov record NCT03782298. 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
Safety and Performance of PEEK Anchors (DYNOMITE, SPYROMITE, RAPTOMITE, FOOTPRINT Ultra PK SL) in Extremities
Study identification
- NCT ID
- NCT03782298
- Recruitment status
- Completed
- Study type
- Observational
- Phase
- Not listed
- Lead sponsor
- Smith & Nephew, Inc.
- Industry
- Enrollment
- 140 participants
Conditions and interventions
Conditions
- Medial or Lateral Instability Repairs/Reconstructions
- Hallux Valgus Repairs
- Achilles Tendon Repairs/Reconstructions
- Midfoot Reconstructions
- Metatarsal Ligament/Tendon Repairs/Reconstructions
- Bunionectomy
- Scapholunate Ligament Reconstructions
- Ulnar
- Lateral Epicondylitis Repair
- Bicep Tendon Reattachments
Interventions
- Spyromite, Dynomite, Raptomite, Footprint Ultra PK SL Device
Device
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Mar 11, 2019
- Primary completion
- Oct 9, 2019
- Completion
- Oct 9, 2019
- Last update posted
- Sep 30, 2024
2019
United States locations
- U.S. sites
- 3
- U.S. states
- 3
- U.S. cities
- 3
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| OrthoCarolina | Charlotte | North Carolina | 28207 | — |
| Precision Orthopaedic Specialties, Inc. | Chardon | Ohio | 44024 | — |
| Foot and Ankle Associates of North Texas-Grapevine | Grapevine | Texas | 76051 | — |
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 1 non-U.S. site.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT03782298, 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 Sep 30, 2024 · Synced Jul 22, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT03782298 live on ClinicalTrials.gov.