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Clinical outcome and implant survival after knee TEP change to triathlon PS and TS systems

Clinical outcome and implant survival after knee TEP change to triathlon PS and TS systems

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00021478
Enrollment
300
Registered
2020-07-02
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

Z96.65 T84

Interventions

Group 1: In this group, patients are asked about implant survival and the revision rate. You have received a total knee endoprosthesis change to the PS system (posterior stabilized prosthesis). Group

Sponsors

Orthopädische Klinik der Medizinischen Hochschule Hannover im Diakovere Annastift
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Male or female patients aged = 18 years - Knee TEP change performed on Stryker Triathlon PS or Triathlon TS prostheses

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
The Primary outcome of this study is to examine implant survival and the revision rate after change operations (KTEP change to PS or TS systems). The different types of implants should be analyzed separately.

Secondary

MeasureTime frame
As a secondary outcome, patient satisfaction and the subjective function of the joint are to be examined in a patient survey using questionnaires. On the other hand, the radiological recordings that have already been made are to be analyzed preoperatively and postoperatively as well as progressive recordings with regard to common radiological criteria of knee arthroplasty (loosening according to the Knee Society Roentgenographic Evaluation and Scoring System - KSRESS, joint and implant position pre- and postoperatively with common axis 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