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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00665210
Other study ID # 2007-511
Secondary ID
Status Recruiting
Phase N/A
First received April 21, 2008
Last updated October 24, 2011
Start date October 2007

Study information

Verified date October 2011
Source Ottawa Hospital Research Institute
Contact Peter Thurston, MD
Phone 613-798-5555
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Observational

Clinical Trial Summary

Hip implants come in different sizes. Currently, surgeons predict the implant size that will be needed using an analogue method whereby photos of the implant sizes are overlaid on the x-rays. In this study, we propose to use a digital, computerized method of templating which we expect will be more accurate than the overlay method.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients booked for primary total hip arthroplasty with non-cemented prosthesis.

- No previous surgery/fractures to acetabulum or femur or hip.

- No gross bony abnormality except for osteoarthritis and avascular necrosis.

Exclusion Criteria:

- Cancer or tumor suspected, morbid obesity, revision, previous acetabular/femur/hip surgery, gross bony deformity, calibration bar not completely pictured on radiograph, unsuccessful surgery fracture/cancer/cemented prosthesis used.

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Canada OHRI Ottawa Ontario

Sponsors (1)

Lead Sponsor Collaborator
Ottawa Hospital Research Institute

Country where clinical trial is conducted

Canada, 

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