Clinical Outcome After Total Knee Arthroplasty Using CR or PS Inlay

NCT03873363 · tracked via the Priya Life Science Germany tracker

Sponsor

Technische Universität Dresden

Phase

Not applicable

Started

2018-04-01

Last updated

2024-02-20

Condition(s) studied

Knee Osteoarthritis

Investigational drug(s) / intervention(s)

PS TKACR TKA

PS TKA: Implantation of a posterior stabilized (cruciate substituting) Total Knee Arthroplasty.

CR TKA: Implantation of a cruciate retaining Total Knee Arthroplasty.

Study summary

Compare knee flexion after cruciate-retaining and cruciate substituting Total Knee Arthroplasty.

Eligibility

Sex

ALL

Min age

18 Years

Max age

—

Healthy volunteers

Inclusion Criteria: * Indication for TKA with a non-linked, bicondylar total knee replacement * written informed consent Exclusion Criteria: * Chronic pain patients * Neuromuscular Diseases * general illnesses that make mobilisation more difficult and/or prevent follow-up * Known posterior cruciate ligament insufficiency * Need for a higher degree of linkage * BMI over 40 kg/m² * Study doctor, his family, employees or other dependent persons

Primary outcome measure(s)

Knee Flexion — 1 year after surgery
Knee flexion measured using a goniometer

Trial sites (1)

Facility	City	Region	Status
University Center of Orthopaedics and Traumatology, University Medicine Carl Gustav Carus Dresden, TU Dresden	Dresden	Saxony

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03873363 on ClinicalTrials.gov ↗ ← All trials in Germany