CT Assessment of Minimally Invasive Surgery and Computer Assisted Navigation in Total Knee Arthroplasty

The recruitment status of this study is unknown because the information has not been verified recently.
Verified December 2006 by Stryker Instruments.
Recruitment status was  Not yet recruiting
Information provided by:
Stryker Instruments
ClinicalTrials.gov Identifier:
First received: December 6, 2006
Last updated: December 7, 2006
Last verified: December 2006
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.

Condition Intervention Phase
Total Knee Replacement
Device: Computer assisted navigation
Phase 4

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment

Further study details as provided by Stryker Instruments:


Ages Eligible for Study:   18 Years to 60 Years
Genders Eligible for Study:   Both

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00409266

Contact: R Scott Oliver, M.D. 781-934-2400 rsolivermd@hotmail.com

United States, Massachusetts
Jordan Hospital Not yet recruiting
Plymouth, Massachusetts, United States, 02360
Principal Investigator: R S Oliver, M.D.         
Sponsors and Collaborators
Stryker Instruments
Principal Investigator: R S Oliver, M.D. Jordan Hospital
  More Information

ClinicalTrials.gov Identifier: NCT00409266     History of Changes
Other Study ID Numbers: NAV06-01US 
Study First Received: December 6, 2006
Last Updated: December 7, 2006
Health Authority: United States: Institutional Review Board

ClinicalTrials.gov processed this record on May 24, 2016