A comparison between total hip replacement surgery using the Modular Dual Mobility prosthesis and Standard Exeter prosthesis with associated precautions
- Conditions
- Hip-joint replacementSurgery
Recruitment & Eligibility
- Status
- Suspended
- Sex
- All
- Target Recruitment
- 100
1. Patients listed for routine primary total hip replacement for osteoarthritis (not trauma)
2. Participants capable of giving informed consent
3. 70 years and over at the time of surgery
4. Suitable for a routine cemented femoral stem and un-cemented acetabular socket
1. Previous hip replacement on contralateral side - (already familiar with precautions)
2. Patient presentation that would not be eligible for a routine implant
3. Patient is unable to comply with the study protocol
4. Inability to understand the patient information for the study, provide written informed consent or answer study questionnaires for cognitive or language reasons
5. Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the study or affect the participant’s ability to participate in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method