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NCT07580157

A Study Of Focused Shockwave For Anterior Knee Pain Following Anterior Cruciate Ligament Reconstruction

Enrolling by Invitation
NAAges 18+InterventionalTreatment
Mayo Clinic
~20 participants
Updated 2026-08-07 on ClinicalTrials.gov
What's tested:Focused ShockwaveSham Focused Shockwave

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Change in International Knee Documentation Committee (IKDC) Subjective Knee Evaluation score
Measured over Baseline, 7 days, 14 days, 21 days, 6 months, 9 months, and 12 months

Conditions

Anterior Cruciate Ligament Injuries

Explore related trials

Anterior knee painInjury of anterior cruciate ligament

NCT07580157

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.

  • Mayo Clinic in Rochester

    Rochester, Minnesotano 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.

Study leadership

  • Joshua M. Romero, M.D. · PRINCIPAL_INVESTIGATOR · Mayo Clinic

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

Want this trial checked against your situation?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

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Eligibility criteria

Inclusion

Adults ≥18 years of age.
Have undergone primary ACL-R with BTB or QT autograft.
Have not previously undergone FSW or radial pressure wave (RPW) in the past for any indication
Must speak English
Capacity to provide consent

Exclusion

Pregnant or breastfeeding.
Revision ACL-R.
History of previous ipsilateral knee surgery.
Multi-ligament knee injury requiring surgical intervention beyond ACL.
History of deep vein thrombosis.
Active infection at or near the harvest site.

What this trial measures

  • Change in International Knee Documentation Committee (IKDC) Subjective Knee Evaluation scoreBaseline, 7 days, 14 days, 21 days, 6 months, 9 months, and 12 months

    The International Knee Documentation Committee (IKDC) Subjective Knee Evaluation is a patient-reported outcome measure focusing on knee symptoms, function, and sports activity. It is scored on a 0-100 scale, where higher scores indicate higher function and lower symptoms.