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NCT04939389: MA-KNEE

Comparing a Sensor for Movement Assessment With Traditional Clinical Assessment Methods in Patients After Knee Surgery.

Completed NA Last updated 9 April 2024
What this trial tests

NA trial testing Orthelligent Pro in Status After Knee Surgery in 36 participants. Completed in 31 May 2022.

Timeline
1 June 2021
Primary endpoint
31 May 2022
31 May 2022

Quick facts

Lead sponsorcrossklinik AG
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment36
Start date1 June 2021
Primary completion31 May 2022
Estimated completion31 May 2022
Sites1 location across Switzerland

Drugs / interventions tested

Conditions studied

Sponsor

crossklinik AG

Who can join

18 and older, any sex, with Status After Knee Surgery. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Eight parameters measurable by the sensor "Orthelligent Pro" are compared with traditional measurements based on a goniometer or video taping. The aim is to inform potential users about the distribution of the differences they have to expect when moving from traditional measurement methods to the new sensor. Patients will perform eight corresponding movement exercises at a single study visit.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Comparing a Sensor for Movement Assessment with Traditional Physiotherapeutic Assessment Methods in Patients after Knee Surgery-A Method Comparison and Reproducibility Study.
    Eymann J, Vach W, Fischer L, Jakob M, et al · · 2022 · cited 2× · PMID 36554461 · DOI 10.3390/ijerph192416581

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Other crossklinik AG trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04939389.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing