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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00409266
Other study ID # NAV06-01US
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date January 2007
Est. completion date June 2007

Study information

Verified date November 2021
Source Stryker Instruments
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The functional flexion axis of the knee can be established by computer-assisted intra-operative data, through range of motion techniques, not specific landmarks such as epicondyles.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date June 2007
Est. primary completion date June 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Males and Females over the age of 18 and equal to or less than the age of 60 - Patients scheduled for elective Total knee arthroplasty surgery - Patients who have signed informed consent and HIPAA Authorization - Able to speak and understand English Exclusion Criteria: - Patients presenting with evidence of recent trauma, active infection, chronic pain syndrome of the spine, dementia or have been diagnosed with Alzheimer's disease - Pregnant women - Patients that will not sign the informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Computer assisted navigation


Locations

Country Name City State
United States Jordan Hospital Plymouth Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Stryker Instruments

Country where clinical trial is conducted

United States, 

References & Publications (1)

Stoeckl B, Nogler M, Krismer M, Beimel C, de la Barrera JL, Kessler O. Reliability of the transepicondylar axis as an anatomical landmark in total knee arthroplasty. J Arthroplasty. 2006 Sep;21(6):878-82. — View Citation

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