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NCT00261066 Clinical Trial

Outcome Following Orthopaedic Surgery

Osteoarthritis of Knee Clinical Trial

Official title:
A Prospective Database for Orthopaedic Surgery

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT00261066
Other study ID # OHREB 2003209-01H
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date May 8, 2003
Est. completion date June 30, 2026

Study information
Verified date November 2023
Source Ottawa Hospital Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

By investigating the long-term functional status of patients who have undergone various types of orthopaedic surgery we will have a basis for devising guidelines for future patients and surgeons.

Description:

The purpose of this database is to explore the long term outcome and functional status of patients undergoing various types of orthopaedic surgery. These data will yield a valuable database that can be used to address future research questions. For example, there are three common surgical treatments for medial osteoarthritis of the knee: tibial osteotomy, Oxford partial knee replacement, or total knee replacement. No clear guidelines exist regarding which treatment options are optimal for which patients. By gathering functional data from patients who have undergone these treatments, we will have a basis for devising such guidelines.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 8439
Est. completion date June 30, 2026
Est. primary completion date June 30, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - All patients who are scheduled to undergo orthopaedic surgery are eligible to be included in the database. Exclusion Criteria: - Those patients who do not meet the above inclusion criteria will be excluded from the study.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Canada Ottawa Hospital Ottawa Ontario

Sponsors (1)
Lead Sponsor Collaborator
Ottawa Hospital Research Institute

Country where clinical trial is conducted

Canada, 

Outcome
Type Measure Description Time frame Safety issue
Primary Koos baseline,1y-2y-5y-7y10y 10y
Secondary ShortForm-12 baseline,1y-2y-5y-7y10y 10Years
Secondary Tegner-ulca baseline,1y-2y-5y-7y10y 10Years
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