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

M

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

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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