CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 50 enrolled
Drug / intervention
Aptus CCS 5.0 or/and 7.0 screwsdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02619838
NCT02619838N/ACompleted
CompareCT.gov

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

Duke University·observational·Posted Dec 2, 2015·Updated Mar 24, 2025

In Brief

An observational study evaluating Aptus CCS 5.0 or/and 7.0 screws for Post-traumatic Osteoarthritis, Unspecified Ankle and Foot and Localized, Primary Osteoarthritis of the Ankle and/or Foot. Completed, enrolled 50 participants across 1 site.

Detailed 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.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsPost-traumatic Osteoarthritis, Unspecified Ankle and Foot, Localized, Primary Osteoarthritis of the Ankle and/or Foot
CountriesUnited States
CollaboratorsMedartis AG

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedDec 2, 2015
Enrollment StartOct 7, 2015
Primary CompletionJan 29, 2024
TodayJul 2, 2026
Enrollment to primary: 8.3 yearsPosted 10.6 years ago

Interventions

Aptus CCS 5.0 or/and 7.0 screwsdevice

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.