Clinical Results of Prophylactic Iodine-supported Primary TKA for Compromised Cases
Not Applicable
- Conditions
- Osteoarthritis, Rheumatoid arthritis of knee joint
- Registration Number
- JPRN-UMIN000033222
- Lead Sponsor
- Fukui General Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
a known allergy or hypersensitivity reaction against iodine based on the medical history simultaneous bilateral or revision TKA
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood serum test Urinary iodine excretion thyroid hormone before surgery and at 1, 6 months, and 1, 3 years after surgery
- Secondary Outcome Measures
Name Time Method postoperative roentgenogram adverse effect