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Clinical Trials in the USA / NCT07688967
Starting soon Observational

Measuring Knee Laxity and Pivot Shift in ACL-Deficient Patients

NCT07688967 · tracked via the Priya Life Science USA tracker
Sponsor
Arthroresearch LLC
Phase
Observational
Started
2026-07-07
Last updated
2026-07-07

Condition(s) studied

Anterior Cruciate Ligament (ACL) Tear

Study summary

The goal of this observational study is to learn whether the Robotic Knee Testing system can measure knee looseness in adults with an anterior cruciate ligament, or ACL, tear.

The main question it aims to answer is whether measurements from the Robotic Knee Testing system are related to the doctor's pivot shift exam grade.

Participants will complete one study visit before ACL reconstruction. During the visit, both knees will be tested in the Robotic Knee Testing system. Researchers may also review existing medical information and imaging.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Adults aged 18-65 years * Confirmed ACL tear by MRI or arthroscopic diagnosis * Able to provide informed consent Exclusion Criteria: * Prior major surgery on the affected knee * Multi-ligament knee injury * Active infection or inflammatory arthropathy * Inability to tolerate passive motion testing * Pregnant or planning to become pregnant during the study period * Unable to provide informed consent

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Trailer Atlanta Georgia
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07688967 on ClinicalTrials.gov ↗ ← All trials in the USA