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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00367289
Other study ID # ctosteolysis-HMO-CTIL
Secondary ID
Status Completed
Phase N/A
First received August 21, 2006
Last updated April 27, 2011
Start date October 2007
Est. completion date December 2008

Study information

Verified date August 2006
Source Hadassah Medical Organization
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial Summary

All patients over 18 who undergo a revision of hip or knee arthroplasty will be included. Patients undergo a CT of the hip joint. A radiologist will mark the presence of cysts and bone loss and will assess implant stability.

After the surgery, the surgeon will fill a similar form.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date December 2008
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients admitted for hip or knee revision arthroplasty

- age over 18

Exclusion Criteria:

- fractures

- dislocations

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Hadassah Medical Organization Jerusalem

Sponsors (1)

Lead Sponsor Collaborator
Hadassah Medical Organization

Country where clinical trial is conducted

Israel, 

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