Mode
Text Size
Log in / Sign up
N/A Completed N=9 Device Feasibility

Clinical Study to Assess the Effectiveness of the Device Patello

Passiv Continuous Patella Mobilisation
Source: ClinicalTrials.gov NCT03512652 ↗
Enrolled (actual)
9
Serious AEs
0.0%
Results posted
Dec 2025
Primary outcomePrimary: Patellofemoral Translation — 0.819; 0.734; 0.776; 0.771 cm

Summary

The device "Patello" was designed to passively mobilize the Patella in cranial-caudal direction. Its application field lays in the rehabilitation of any knee pathology where knee range of motion may be restricted due to the Patella mobility.

Outcome Measures

OutcomeResultp-value
PRIMARY
Patellofemoral Translation
0.819; 0.734; 0.776; 0.771; 0.774

Eligibility Criteria

Inclusion Criteria

  • no operation and / or actual problems (pain at rest or during strain) of the muscular or bony parts of the lower extremities
  • closed and intact skin conditions in the area of the knees and thighs
  • no fear of the intervention
  • willingness to participate on all 2 measurement days

Exclusion Criteria

  • operation and / or actual problems (pain at rest or during strain) of the muscular or bony parts of the lower extremities
  • open skin conditions in the area of the knees and thighs
  • fear of the intervention
  • no willingness to participate on all 2 measurement days
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03512652). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

Back to search