Using Cryoneurolysis to Reduce Pain After ACL Surgery
The Effect of Pre-Operative Cryoneurolysis on Post-Operative Narcotic Consumption in Patients Undergoing Autograft ACL Reconstruction
This study is testing if using extreme cold on specific nerves before ACL surgery can help reduce pain and the need for pain medication afterward.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 14 Years and up |
| Sex | All |
| Sponsor | Virtua Health, Inc. Academic / other |
| Locations | 2 sites (Burlington, New Jersey and 1 other locations) |
| Trial ID | NCT06603051 on ClinicalTrials.gov |
What this trial studies
This research investigates the impact of preoperative Cryoneurolysis on pain management for patients undergoing autograft anterior cruciate ligament (ACL) reconstruction. Participants will be randomly assigned to receive either standard care or standard care plus Cryoneurolysis, which involves applying extreme cold to targeted nerves to alleviate pain. The study aims to determine if this additional treatment can reduce postoperative narcotic consumption. Both groups will receive standard pain management protocols during and after the surgery.
Who should consider this trial
Good fit: Ideal candidates are patients aged 14 and over who are opioid naïve and undergoing autograft ACL reconstruction.
Not a fit: Patients under 14, those who are non-English speaking, or those with certain medical conditions such as Reynaud's syndrome or skin disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce the need for narcotics after ACL surgery, leading to better pain management and fewer side effects associated with opioid use.
How similar studies have performed: While the use of Cryoneurolysis is established, this specific application in ACL reconstruction is novel and has not been extensively tested in prior studies.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Burlington, New Jersey and 1 other locations
- Virtua Orthopedics Burlington — Burlington, New Jersey, United States (Recruiting)
- Virtua Orthopedics Cherry Hill — Cherry Hill, New Jersey, United States (Recruiting)
Study contacts
- Study coordinator: Sean Mc Millan, DO
- Email: smcmillan@virtua.org
- Phone: (609)747-9200
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.