Robotic assisted versus manually instrumented total knee revision arthroplasty- a randomized, controlled trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00036659

Enrollment

100

Registered

2025-06-27

Start date

2025-04-21

Completion date

Unknown

Last updated

2025-10-06

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

Conditions

T84.05

Interventions

Group 1: Patients who received robotic-assisted total knee arthroplasty revision. The following data will be collected: • Demographic data (age, gender, height, weight, BMI, ASA score) • Diagnosis an

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Written consent for participation in the study Planned single stage total knee arthroplasty revision using a non-hinged implant type

Exclusion criteria

Exclusion criteria: Patients who did not consent to participate Patients who are not able to consent because of mental disabilities or lack or a language barrier Revision due to a tumor or infection Revision to a hinged-type implant

Design outcomes

Primary

Measure	Time frame
Pre- and postoperative radiographic measurements, functional outcome and patient reported outcome measures with follow-up appointments of 12 months, 2 and 5 years after surgery.	—

Secondary

Measure	Time frame
Patient satisfaciton	—

Countries

Germany

Contacts

Public ContactHendrik Pott

Pius-Hospital Oldenburg

hendrik.pott@pius-hospital.de04412291561

Outcome results

None listed

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