Clinical trial for bone union of allografts in periprosthetic femoral fracture of total hip arthroplasty by LIPUS
Not Applicable
- Conditions
- periprosthetic femoral fracture of total hip arthroplasty
- Registration Number
- JPRN-UMIN000002406
- Lead Sponsor
- Department of Orthopaedics, Kyoto University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Not provided
Exclusion Criteria
(1)The patient receiving LIPUS treatment or electrical stimulation before. (2)The patient who is unable to apply LIPUS treatment. (3)The patient had recent severe systemic past history such as heart, liver or kidney disease. (4)The patient had abnormal skin sensitivity or sensory paralysis. (5)The patient had unhealed skin injury. (6)The patient had treated cancer therapy within recent five years. (7)The patient is pregnant or possible pregnant. (8)The patient who is unable to comply with this study protocol spontaneuosly. (9)The patient who is unable to comply with the consent form of this study . (10)The patient who was recognized unsuitable for this study by primary physician.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluation of the period of callus formation and bone union after operation by radiograph
- Secondary Outcome Measures
Name Time Method