Unique ID issued by UMIN | UMIN000032886 |
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Receipt number | R000035964 |
Scientific Title | A pilot study of a simple navigation system for total knee arthroplasty using augmented reality technology |
Date of disclosure of the study information | 2018/06/20 |
Last modified on | 2018/08/24 13:15:28 |
A pilot study of a simple navigation system for total knee arthroplasty using augmented reality technology
A pilot study of a simple navigation system for total knee arthroplasty using augmented reality technology
A pilot study of a simple navigation system for total knee arthroplasty using augmented reality technology
A pilot study of a simple navigation system for total knee arthroplasty using augmented reality technology
Japan |
Patients with knee joint disease who are scheduled to undergo total knee arthroplasty(TKA) (osteoarthritis, rheumatoid arthritis, knee osteonecrosis).
Orthopedics |
Others
NO
To assess the safety and efficacy of TKA using mix-augmented reality technology in patients with knee joint disease who are scheduled to undergo TKA.
Safety,Efficacy
Difference between 3D pre-operative planning and post-operative implantation (by tibial component, internal and external rotation).
Difference between 3D pre-operative planning and post-operative implantation (by other than tibial component, internal and external rotation).
Adverse event.
Device deficiency.
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Treatment
Device,equipment |
Using patient specific guide linked with 3D surgical support software for TKA
20 | years-old | <= |
Not applicable |
Male and Female
(1) Patients with knee joint disease (osteoarthritis, rheumatoid arthritis, knee osteonecrosis).
(2) Patients who are scheduled to undergo TKA.
(3) Patients aged 20 years or older at the time of acquiring consent.
(4) Document consent can be obtained by the patient's free will, after receiving sufficient explanation for the participation of this study, after understanding.
(1) Patients who have been registered in this study in the past.
(2) Patients with or suspected to have Creutzfeldt-Jakob disease.
(3) Patients judged by the principal investigator to be inappropriate as subjects.
3
1st name | |
Middle name | |
Last name | Daihei Kida |
National Hospital Organization Nagoya Medical Center
Orthopedic Surgery and Rheumatology
4-1-1 Sannomaru, Naka-ku, Nagoya-shi, Aichi, 460-0001, Japan
052-951-1111
kidad@nnh.hosp.go.jp
1st name | |
Middle name | |
Last name | Daihei Kida |
National Hospital Organization Nagoya Medical Center
Orthopedic Surgery and Rheumatology
4-1-1 Sannomaru, Naka-ku, Nagoya-shi, Aichi, 460-0001, Japan
052-951-1111
kidad@nnh.hosp.go.jp
National Hospital Organization Nagoya Medical Center
National Hospital Organization Nagoya Medical Center
Self funding
NO
独立行政法人 国立病院機構
名古屋医療センター
2018 | Year | 06 | Month | 20 | Day |
Unpublished
No longer recruiting
2018 | Year | 04 | Month | 20 | Day |
2018 | Year | 06 | Month | 20 | Day |
2018 | Year | 06 | Month | 06 | Day |
2018 | Year | 08 | Month | 24 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000035964
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