NCT07171346
Post Operative Use of Neuromuscular Electrical Stimulation (NMES) Device for ACLR Patients
Enrolling by Invitation
NAAges 15–50InterventionalTreatmentUniversity of Kansas Medical CenterInvestigator-initiated
~25 participants
Updated 2026-03-17 on ClinicalTrials.gov
What's tested:Zynex NexWave Electrotherapy Device
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Bilateral Muscle Symmetry Index
Measured over pre-operative to 3 months post-op
Conditions
NCT07171346
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
University of Kansas Medical Center
Kansas City, Kansasno site contact published
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
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Eligibility criteria
Inclusion
ACLR surgical patients at KUMC sports medicine
15 to 50 years old
BMI between 18 - 30 kg/m2
No limitations impacting physical function within the last 6 months (not including the ACL injury)
Exclusion
Previous lower limb or spine injury involving surgical treatment
Prior spine surgery
Lower limb injury (other than ACL) preventing participation in physical activity for over two weeks in the past 6 months
Non english speaking
Vulnerable population, prisoner, or ward of the state
What this trial measures
- Bilateral Muscle Symmetry Indexpre-operative to 3 months post-op
Comparing muscle size strength and function between operative and non-operative limbs