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NCT01017562 Clinical Trial

Differentiation of Aseptic From Septic Loosening by 18F-fluoride PET

Hip Arthroplasty Clinical Trial

Official title:
Differentiation of Aseptic From Septic Loosening in Patients With Total Hip Arthroplasty Using 18F-fluoride PET

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01017562
Other study ID # YCU21-106
Secondary ID
Status Completed
Phase N/A
First received November 19, 2009
Last updated November 19, 2009
Start date April 2007
Est. completion date November 2009

Study information
Verified date November 2009
Source Yokohama City University Medical Center
Contact n/a
Is FDA regulated No
Health authority Japan: Institutional Review Board
Study type Observational

Clinical Trial Summary

In this study, the investigators utilized the 18F-fluoride PET method to evaluate THA cases with a stable, septic or septic loosened implant in order to differentiate these clinical settings using a novel uptake type classification approach.

Recruitment information / eligibility
Status Completed
Enrollment 61
Est. completion date November 2009
Est. primary completion date September 2009
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Exclusion Criteria:

- Within one year after surgery

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Japan Departement of orthopaedic sugery Yokohama Kanagawa

Sponsors (1)
Lead Sponsor Collaborator
Yokohama City University Medical Center

Country where clinical trial is conducted

Japan, 

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