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Study identifier: NCT06603051 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Recruiting

The Effect of Pre-Operative Cryoneurolysis on Post-Operative Narcotic Consumption in Patients Undergoing Autograft ACL Reconstruction

Condition: ACL Repair  ·  Sponsor: Virtua Health, Inc.

PhaseNA
Planned participants20
Who can joinAll sexes, 14 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where2 locations

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

The purpose of the research is to investigate the effect of preoperative Cryoneurolysis of the knee on postoperative pain management in patients undergoing autograft anterior cruciate ligament (ACL) reconstruction (a surgical procedure that makes a new ACL using the patient's own tendon). Cryoneurolysis is an approved process of applying extreme cold temperatures to targeted nerves in order to decrease or eliminate pain. . If you take part in the research, you will be randomly assigned (assigned by chance, like a flip of a coin) to Group A (standard care) or Group B (standard care plus Cryoneurolysis). Participants in both groups will undergo standard ACL reconstruction and receive standard preoperative and postoperative pain management. Participants in Group B only will also receive a standard treatment of Cryoneurolysis to their surgical knee within 7-10 days before their scheduled surgery. Participants in both groups (A \& B) will be asked to bring their remaining postoperative pain medication to their postoperative follow-up appointments for review by study personnel. Participants will also be asked to complete a survey about their knee activity, function and symptoms at these appointments. Your time in the study will last until the completion of the 12-week postoperative follow-up appointment.

This description comes directly from the study's public registry record.

Talk to the study team

Sean Mc Millan, DO  ·  (609)747-9200  ·  smcmillan@virtua.org

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * \- Patients aged 14 and over * Patients who are patients within the PI's practice * Patients who can speak and read English * Patients undergoing autograft ACL reconstruction. * Patients who are opioid naïve Exclusion Criteria: * \- Under the age of 14 * Non-English speaking/reading patients * Patients with Reynauds' syndrome * Patients with skin disorders or hypo-vascularity * Patients undergoing allograft ACL reconstruction. * Patients who consistently use opioids preoperatively

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (2)

Virtua Orthopedics BurlingtonBurlington, New Jersey, United StatesRecruiting
Virtua Orthopedics Cherry HillCherry Hill, New Jersey, United StatesRecruiting

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