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Time-dependent Improvement of Functional Outcome Following LCS Rotating Platform TKR

NCT ID: NCT01030848

Last Updated: 2009-12-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2003-02-28

Study Completion Date

2013-09-30

Brief Summary

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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 four years following TKR using the LCS rotating platform prosthesis. Improvement of patient self-reported pain and daily function during the study period, are of particular interest.

Detailed Description

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Conditions

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Osteoarthritis Total Knee Replacement

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients with knee osteoarthritis

Total Knee Replacement (LCS rotating platform)

Intervention Type DEVICE

Interventions

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Total Knee Replacement (LCS rotating platform)

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* patients with knee osteoarthritis
* admitted for total knee replacement
* no rheumatoid arthritis
* no previous knee infection
* age 40-85 years

Exclusion Criteria

\-
Minimum Eligible Age

40 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Martina Hansen's Hospital

OTHER

Sponsor Role lead

Responsible Party

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Martina Hansens Hospital

Principal Investigators

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Tor Kjetil Nerhus, MD

Role: PRINCIPAL_INVESTIGATOR

Martina Hansens Hospital

Locations

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Martina Hansens Hospital

Bærum, Bærum, Norway

Site Status

Countries

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Norway

Other Identifiers

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19039 (NSD)

Identifier Type: REGISTRY

Identifier Source: secondary_id

TKN-001

Identifier Type: -

Identifier Source: org_study_id