Combined unicompartmental knee arthroplasty (UKA) and anterior cruciate ligament (ACLR) study

Completed

• Conditions: nicompartmental knee arthroplasty and anterior cruciate ligament reconstruction; Musculoskeletal Diseases

• Registration Number: ISRCTN24663935
• Lead Sponsor: The Affiliated Hospital of Qingdao University

Brief Summary

2016 results in: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974734

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2014-01-01
• Study Start: 2016-07-21
• Last Update Posted: 19 March 2018

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 25

Inclusion Criteria

Patients with isolated medial femorotibial compartment OA secondary to ACL deficiency and primary isolated medial femorotibial OA with acute ACL injury.

Exclusion Criteria

1. Severe knee OA apart from the femorotibial compartment
2. Multiple ligment injuries

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. Patient assessment of levels of, and change in, pain and function of the knee, using the Oxford Knee Score (OKS)<br>2. Clinical profile (pain intensity, range of motion and stability in the anteroposterior and mediolateral planes, flexion deformities, contractures and poor alignment. ), using KSS-clinical score and KSS-function score<br>3. Activity levels for daily living, using the Tegner activity score<br>4. Radiological assessment<br><br>Measured before surgery, and then 3, 6, 12 and 24 months after surgery

Secondary Outcome Measures

Name	Time	Method
Post-operative range of movement, assessed using the KT-2000 arthrometer test, measured before surgery and then 3, 6, 12 and 24 months after surgery