DEXA Bone Density Analysis of the CoreHip® Prosthesis System
This trial has no sites in United States.
It has sites in one country. Choose a country to see its sites.
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 35 and 85 years old?
Source: NCT06632301, who can take part
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- Aesculap AG
- Trial code
- NCT06632301
- Record updated
- 16 October 2026
- Original description
The goal of this interventional post-market follow-up study is to evaluate radiological changes in the diaphyseal bone density (Gruen Zones 3 and 4) within 24 months postoperative in patients treated with CoreHip® primary cementless stem. The DEXA bone density analysis is used.Read full original descriptionShow less
DEXA Bone Density Analysis to Analyze the Loading Concept of the CoreHip® Prosthesis
The goal of this interventional post-market follow-up study is to evaluate radiological changes in the diaphyseal bone density (Gruen Zones 3 and 4) within 24 months postoperative in patients treated with CoreHip® primary cementless stem. The DEXA bone density analysis is used.
Inclusion: Unilateral hip osteoarthritis; Indication for CoreHip Standard hip stem according to preoperative planning; Written Informed Consent; Age 35-85 years; According to the assessment of the study doctor, the patient is therapy compliant and able to attend the follow-up visits.
Exclusion: History of femoral fracture or previous surgery on the same hip; Metabolic bone disease, use of steroids or other drugs affecting bone metabolism; Femoral neck fractures; Pregnancy; BMI > 35; Intraoperative bone cracks; Severe osteoarthritis of the contralateral hip; THA of the contralateral side or other event leading to restricted weight bearing during the study period.