Substitution of the PCL in TKA With UC or PS Design

Technische Universität Dresden

Status: Active, not recruiting

Conditions: Knee Arthroplasty; Patient Reported Outcome; Knee Osteoarthritis

Treatments: Other: TKA

Study type: Interventional

Funder types: Other

Identifiers

NCT04679857

TKA UC PS

Details and patient eligibility

About

RCT comparing UC and PS TKA

Full description

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

Enrollment: 127 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• scheduled for TKA

Exclusion criteria

• higher constraint needed

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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127 participants in 2 patient groups

UC

Experimental group

Description:

Total Knee Arthroplasty with an ultracongruent insert

Treatment:

Other: TKA

PS

Active Comparator group

Description:

Total Knee Arthroplasty with posterior stabilized design

Treatment:

Other: TKA