Skip to content

Clinical outcome and implant survival after knee TEP change with the use of bone replacing implants

Clinical outcome and implant survival after knee TEP change with the use of bone replacing implants

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00021481
Enrollment
100
Registered
2020-07-20
Start date
2026-12-31
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

M17.9 Z96.65

Interventions

Group 1: Patients who have been operated on using cones as a bone-replacing implant system. Initially, the respective patients will be contacted by telephone by the physicians in order to be informed

Sponsors

Medizinische Hochschule Hannover
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Male or female patients in the age group = 18 years - Performed surgery using cones, sleeves or wedges as bone-replacing implant systems

Exclusion criteria

Exclusion criteria: Renewed revision of the knee TEP with replacement of individual or all components

Design outcomes

Primary

MeasureTime frame
The primary objective of this study is to investigate the respective revision rates and the respective implant survival after a change operation using the implant systems cones, sleeves and wedges.

Secondary

MeasureTime frame
As a secondary objective, patient satisfaction and the subjective function of the joint will be investigated by means of questionnaires within the framework of a patient survey. On the other hand, the radiological images already taken pre- and postoperatively as well as follow-up images will be analyzed with regard to common radiological criteria of knee endoprosthetics (loosening according to Knee Society Roentgenographic Evaluation and Scoring System - KSRESS, joint and implant position pre- and postoperatively with common axial angles).

Countries

Germany

Contacts

Public ContactYvonne Noll

Orthopädische Klinik der Medizinischen Hochschule Hannover im Diakovere Annastift, Leitung Klinisches Studienmanagement

yvonne.noll@diakovere.de0511-5354-649

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Apr 4, 2026