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Clinical Trial

DEXA Bone Density Analysis of the CoreHip® Prosthesis System

NCT: NCT06632301 · NOT_YET_RECRUITING

NCT IDNCT06632301

StatusNOT_YET_RECRUITING

SponsorAesculap AG (INDUSTRY)

First posted2024-10-09

Last updated2026-08-20

Brief Summary

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.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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