Patient reported clinical outcomes and imaging study for a new all-ceramic hip resurfacing device

Not Applicable

• Conditions: End-stage joint disease e.g. osteoarthritis, requiring hip joint replacement; Musculoskeletal Diseases

• Registration Number: ISRCTN93110271
• Lead Sponsor: MatOrtho Limited

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-10-15
• Last Update Posted: 27 May 2024
• Study Completion: 2027-03-31

Recruitment & Eligibility

• Status: Ongoing
• Sex: All
• Target Recruitment: 78

Inclusion Criteria

1. Patient suitable for hip resurfacing arthroplasty
2. Patient able to give informed consent
3. Patient willing and able to take part in the study for the prescribed length of the study
4. Willing to allow his or her General Practitioner and consultant, if appropriate, to be notified of participation in the study
5. Minimum age of 18 years

Exclusion Criteria

1. Patient deemed unsuitable for hip resurfacing arthroplasty by the surgeon
2. Patient has significant contraindications when following the manufacturer's Instruction For Use of the product
3. Patient likely to become incapacitated during the study
4. 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 may influence the result of the study, or the participant’s ability to participate in the study

Study & Design

• Study Type: Observational
• Study Design: Not specified