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NCT02358447 Clinical Trial

SPECT-CT for Assessment of Total Knee Arthroplasty in Navigated and Non-navigated Total Knee Arthroplasty

Osteoarthritis Clinical Trial

Official title:
SPECT-CT for Assessment of Patients Before and After Navigated and Conventional Total Knee Arthroplasty.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02358447
Other study ID # SPECT/CT-TKR_001_MH
Secondary ID 380/09
Status Completed
Phase
First received
Last updated
Start date April 2010
Est. completion date October 23, 2018

Study information
Verified date October 2018
Source Kantonsspital Baselland Bruderholz
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

By the comparison of two operation methods navigated and non-navigated TKR with SPECT/CT we want to show wich method has the better outcome.

Description:

With SPECT/CT we want to controll the clinical outcome of patients who underwent a navigated or a non-navigated TKR.

Recruitment information / eligibility
Status Completed
Enrollment 210
Est. completion date October 23, 2018
Est. primary completion date July 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Total Knee prosthesis (primary)

- >18 years

Exclusion Criteria:

- pregnancy

- lactating women

- endocrine diseases

- tumour diseases

- posttraumatic osteoarthritis of the knee

- previous infection of the knee

- medicaments which influence the metabolism of the bone

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• TKR
non-navigated versus computer-navigated total knee replacement

Locations
Country Name City State
Switzerland Kantonsspital Baselland, Bruderholz Bruderholz Baselland

Sponsors (1)
Lead Sponsor Collaborator
Kantonsspital Baselland Bruderholz

Country where clinical trial is conducted

Switzerland, 

Outcome
Type Measure Description Time frame Safety issue
Primary which operation method is the best in terms of outcome and SPECT/CT imaging five years
Secondary Improvement in the post-treatment five years
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