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Clinical Trials/NCT04679857
NCT04679857
Active, not recruiting
Not Applicable

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

Technische Universität Dresden1 site in 1 country127 target enrollmentNovember 1, 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Patient Reported Outcome
Sponsor
Technische Universität Dresden
Enrollment
127
Locations
1
Primary Endpoint
Patient reported outcome
Status
Active, not recruiting
Last Updated
2 years ago

Overview

Brief Summary

RCT comparing UC and PS TKA

Detailed Description

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

Registry
clinicaltrials.gov
Start Date
November 1, 2012
End Date
December 30, 2025
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • scheduled for TKA

Exclusion Criteria

  • higher constraint needed

Outcomes

Primary Outcomes

Patient reported outcome

Time Frame: 10 years

Oxford Knee Score min 0 points (worst), max 48 points (best)

ROM

Time Frame: 10 years

Range of motion

Study Sites (1)

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