Non-Interventional, Multicenter Bicontact® E PMCF Study
- Conditions
- Femoral Neck FracturesFemoral Head NecrosisDegenerative OsteoarthritisRheumatoid Arthritis
- Registration Number
- NCT03442855
- Lead Sponsor
- Aesculap AG
- Brief Summary
Prospective observational (non-interventional) cohort study, multi-centric in 5 study Centers in Japan to collect short term clinical and radiological results of the cementless Bicontact® E stem in a standard patient population used in routine clinical practice
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 73
- Indication for Bicontact E prosthesis THA
- Patients ≥ 18 years
- Patient not pregnant
- Written informed consent
- Patients receiving a bipolar implantation
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical Results 1 year Hip Score of the Japanese Orthopaedic Association (JOA): three categories-movement, mental, and pain-each comprising 7 items, for a total of 21 items to be used as evaluation criteria for hip-joint function
- Secondary Outcome Measures
Name Time Method Thigh Pain 1 year Pain as measured with the Visual Analog Scale (VAS): Visual analog scale \[VAS\] is a measure of pain intensity. It is a continuous scale comprised of a horizontal analog scale of 100 mm length. It is anchored by two verbal descriptors, one for each symptom extreme \[no pain - worst imaginable pain\].
X-Ray evaluation 1 year Radiological results (osteointegration, migration)
(Serious) Adverse Events 1 year Complications: Adverse Events (AE) / Serious Adverse Events (SAE)
Trial Locations
- Locations (5)
Funabashi Orthopedic Hospital
🇯🇵Funabashi, Japan
Niigata Bandai Hospital
🇯🇵Niigata, Japan
Niigata Rinko Hospital
🇯🇵Niigata, Japan
Niigata Univ. Medical & Dental Hospital
🇯🇵Niigata, Japan
Saiseikai Niigata Second Hospital
🇯🇵Niigata, Japan