← Back to Clinical Trials
Recruiting NCT06626490

NCT06626490 Prospective Follow-up of the Prevision Hip Stem With Comparison of Different Implant Variants

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06626490
Status Recruiting
Phase —
Sponsor Aesculap AG
Condition Revision Total Hip Arthroplasty
Study Type OBSERVATIONAL
Enrollment 120 participants
Start Date 2026-04-07
Primary Completion 2033-03

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Prevision Revision hip endoprosthesis stem implantation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 120 participants in total. It began in 2026-04-07 with a primary completion date of 2033-03.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The study design is confirmative for non-inferiority of the functional outcome of the implants and is intended to examine the safety and performance of the Prevision hip stem. The study is an observational post-market clinical follow-up study, and the study sites chose the stem variant depending on their own routine and indication.

Eligibility Criteria

Inclusion Criteria: * Revision hip arthroplasty patients treated with a Prevision hip stem * Written patient informed consent * Patients are able to attend at follow-up examinations Exclusion Criteria: * Patients \< 18 years at surgery * Pregnancy at implantation * Patients held in a custodial setting * Patients in a relationship of dependence on the sponsor, the clinic or the investigator

Contact & Investigator

Central Contact

Kerstin Bergmann

✉ studies@aesculap.de

📞 +49746195-

Principal Investigator

Henning Windhagen, Prof. Dr.

PRINCIPAL INVESTIGATOR

Orthopädische Kliniken im Annastift, MHH

Frequently Asked Questions

Who can join the NCT06626490 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Revision Total Hip Arthroplasty. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06626490 currently recruiting?

Yes, NCT06626490 is actively recruiting participants. Contact the research team at studies@aesculap.de for enrollment information.

Where is the NCT06626490 trial being conducted?

This trial is being conducted at Hanover, Germany, Huntingdon, United Kingdom.

Who is sponsoring the NCT06626490 clinical trial?

NCT06626490 is sponsored by Aesculap AG. The principal investigator is Henning Windhagen, Prof. Dr. at Orthopädische Kliniken im Annastift, MHH. The trial plans to enroll 120 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology