Outcome EnduRo Versus LINK SL Rotating Hinge Knee

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01952938

Enrollment

Registered

2013-09-30

Start date

2012-07-31

Completion date

Unknown

Last updated

2013-09-30

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

Conditions

Knee Arthrosis,

Keywords

knee revision surgery,, rotating hinge prosthesis

Brief summary

Randomized clinical outcome study of two rotating hinge knee prosthesis in knee surgery. Hypothesis: No difference in the clinical outcome for 1 year after the operation. Clinical follow-ups at 3, 10, 90 and 360 days after surgery. Measurement of clinical parameters

Interventions

PROCEDURELINK SL versus EnduRo

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Yes

Inclusion criteria

* rotating hinge knee indicated

Exclusion criteria

* infection, * malignant tumor, * rheumatism

Design outcomes

Primary

Measure	Time frame
Oxford knee score	one year

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026