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Retrospective Foot and Ankle Data Collection

NCT05234801 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2022-05-24

No results posted yet for this study

Summary

A retrospective post-market data collection study of the following implant devices :

* DARCO™ Headed Cannulated Screw
* ORTHOLOC™ 3Di Recon-Midfoot/Flatfoot System
* ORTHOLOCTM 3Di 2 Foot Reconstruction System: CROSSCHECK™ Module

Conditions

  • Lower Limb Surgery

Interventions

DEVICE

DARCO™ Headed Cannulated Screw

The DARCO™ Headed Cannulated Screw is a multi-size screw system designed to be used over a guide pin or wire with instrumentation to provide interfragmentary compression and stability for bone fracture/fragment fixation.

DEVICE

ORTHOLOC™ 3Di Recon-Midfoot/Flatfoot System

A multi-indication foot reconstruction solution providing indication specific implants and instruments designed to address the unique demands of the forefoot and midfoot.

DEVICE

ORTHOLOCTM 3Di 2 Foot Reconstruction System: CROSSCHECK™ Module

A comprehensive fixation system consisting of a wide variety of plate options, created with the purpose of stabilization and fixation of fractures, revision procedures, joint fusion and reconstruction of small bones of the feet.

Sponsors & Collaborators

  • Robert Jones and Agnes Hunt Orthopaedic and District NHS Trust

    lead OTHER_GOV

Principal Investigators

  • Andrew Bing, FRCS · Robert Jones and Agnes Hunt Orthopaedic Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-03-30
Primary Completion
2022-06-30
Completion
2022-07-30

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05234801 on ClinicalTrials.gov