Clinical study of a novel artificial wrist joint(NM002)
- Conditions
- Rheumatoid arthritis
- Registration Number
- JPRN-UMIN000002991
- Lead Sponsor
- Hokkaido University Hospital Orthopedics
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 20
Not provided
(1)Patient who has previously experienced the the wrist joint arthropathy. (2)Patient who was diagnosed as neuropathic arthropathy. (3)Patient who has an evident or a possible infection in or around the wrist joint. (4)Patient who has a mental illness and is considered not to obey directions of the doctor. (5)Patient who is pregnant or possibly pregnant. (6)Patient who is considered not to receive aftercare by the directions of the doctor. (7)Patient who is participating in an another clinical study. (8)Patient who has been previously implanted with the test device NM002. (9)Patient in whom the test device is not expected to be fixed firmly due to poor volume of bone, or in whom functional recovery of the wrist is not expected due to difficulty of the reconstruction of tendon. (10)Patient who has experienced serious advers reaction(s) caused by bone cement, sach as decrease in blood pressure, shock, or pulmonary embolism. (11)Patient who is determined to be excluded from the study due to any reason by the study doctor.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method