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NCT04956315

Accuracy and Stability of a New Automatic Knee Arthrometer in Diagnosing ACL Rupture

Completed Last updated 9 July 2021
What this trial tests

trial testing Side-to-side difference (reproducibility) in Knee Ligament; Laxity in 421 participants. Completed in 31 December 2020.

Timeline
30 June 2020
Primary endpoint
1 July 2020
31 December 2020

Quick facts

Lead sponsorPeking University Third Hospital
StatusCompleted
Study typeOBSERVATIONAL
Enrollment421
Start date30 June 2020
Primary completion1 July 2020
Estimated completion31 December 2020
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Peking University Third Hospital

Who can join

Adults 18 to 45, any sex, with Knee Ligament; Laxity. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

We introduced an automatic knee arthrometer (AKA) and aimed to evaluate the repeatability and effectiveness thereof in diagnosing ACL rupture compared with the KT-2000.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Peking University Third Hospital trials

Trials by the same sponsor.

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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/NCT04956315.

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