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NCT04679857 Clinical Trial

Substitution of the PCL in TKA With UC or PS Design

Knee Osteoarthritis Clinical Trial

Official title:
Substitution of the Posterior Cruciate Ligament in Total Knee Arthroplasty With Ultracongruent Insert or Posterior Stabilzed Design

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT04679857
Other study ID # TKA UC PS
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date November 1, 2012
Est. completion date December 30, 2025

Study information
Verified date February 2024
Source Technische Universität Dresden
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

RCT comparing UC and PS TKA

Description:

RCT comparing TKA with either ultraconguent insert or posterior stabilized design for substitution of the posterior cruciate ligament

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 127
Est. completion date December 30, 2025
Est. primary completion date March 30, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - scheduled for TKA Exclusion Criteria: - higher constraint needed

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• TKA
Total Knee Arthroplasty

Locations
Country Name City State
Germany University Center of Orthopaedics and Traumatology, University Medicine Carl Gustav Carus Dresden, TU Dresden Dresden Saxonia

Sponsors (1)
Lead Sponsor Collaborator
Technische Universität Dresden

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary ROM Range of motion 10 years
Primary Patient reported outcome Oxford Knee Score min 0 points (worst), max 48 points (best) 10 years
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