Time-dependent Improvement of Functional Outcome Following Oxford Medial Unicondylar Knee Replacement

Martina Hansen's Hospital

Status: Completed

Conditions: Osteoarthritis

Study type: Observational

Funder types: Other

Identifiers

NCT01032538

TKN-002

19441 (NSD) (Registry Identifier)

Details and patient eligibility

About

The objective of this prospective study is to determine (1) the time course of patient-relevant functional outcome evaluated by the Knee injury and Osteoarthritis Outcome Score (KOOS) and (2) the time course of range of motion (ROM) the first six years following Oxford Medial Unicondylar Knee prosthesis. Improvement of patient self-reported pain and daily function during the study period, are of particular interest.

Full description

The objective of this prospective study is to determine (1) the time course of patient-relevant functional outcome evaluated by the Knee injury and Osteoarthritis Outcome Score (KOOS) and (2) the time course of range of motion (ROM) the first six years following Oxford Medial Unicondylar Knee prosthesis. Improvement of patient self-reported pain and daily function during the study period, are of particular interest. Thats it!

Enrollment: 99 patients

Sex: All

Ages: 50 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• patients with medial knee osteoarthritis
• admitted for unicondylar knee replacement
• age 50-80 years

Exclusion criteria

• rheumatoid arthritis
• previous knee infection

Trial design

99 participants in 1 patient group

Patients with knee osteoarthritis

Description:

Patients with knee osteoarthritis that are about to get an operation with oxford unicondylar knee