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Prospective Subtalar, Double, or Triple Arthrodesis Study With CCS Screws

NCT02619838 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2025-03-24

Study results available
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Summary

The objective of this study is to prospectively evaluate the mid-term results and intraoperative and postoperative complication rate in patients who underwent double or triple arthrodesis using CCS screws.

Conditions

  • Post-traumatic Osteoarthritis, Unspecified Ankle and Foot
  • Localized, Primary Osteoarthritis of the Ankle and/or Foot

Interventions

DEVICE

Aptus CCS 5.0 or/and 7.0 screws

Fusion of the talonavicular joint, the subtalar joint, and the calcaneal-cuboid joint with a Aptus CCS screws. The assignment of the device is at the discretion of the standard of care provider, not the study investigator.

Sponsors & Collaborators

Principal Investigators

  • Mark E. Easley, MD · Duke Health

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-10-07
Primary Completion
2024-01-29
Completion
2024-01-29

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT02619838 on ClinicalTrials.gov