CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 21 enrolled
Drug / intervention
Klassic Knee Systemdevice
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/NCT04113785
NCT04113785N/ACompleted

In Vivo Kinematics for Subjects Implanted With Klassic TKA

The University of Tennessee, Knoxville·observational·Posted Oct 3, 2019·Updated Nov 15, 2019

In Brief

An observational study evaluating Klassic Knee System for Total Knee Arthroplasty and 3 related conditions. Completed, enrolled 21 participants across 1 site.

Detailed Summary

In vivo knee kinematics will be assessed for 20 subjects that have been implanted with a Total Joint Orthopedics Klassic knee system by Dr. Aaron Hofmann of the Hofmann Arthritis Institute's Center for Precision Joint Replacement. This is the location from which all participants will be recruited and where fluoroscopy data collection will occur. Participants will undergo fluoroscopic surveillance of their implanted knee using a C-arm fluoroscopic unit while performing a deep knee bend activity at least six months post-operatively.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedOct 3, 2019
Enrollment StartOct 1, 2018
Primary CompletionDec 31, 2018
Study CompletionJun 5, 2019
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 6.7 years ago

Interventions

Klassic Knee Systemdevice

At present, all TKA available for surgeons to use are asymmetric where there is a distinct femoral and tibial component for the left knee and a distinct femoral and tibial component for the right knee. The Klassic knee system is a symmetrical knee implant, where the same femoral and same tibial component can be used for either the right or left knee