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VibraCool Device to Reduce Pain and Opioid Use After Anterior Cruciate Ligament Reconstruction (ACLR)

Columbia University · NCT06456268

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Any age listed · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
130
US sites recruiting
1
Study start
June 2026
Record last updated
January 7, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

The goal of this project is to test the effects of the VibraCool mechanical stimulation neuromodulatory therapeutic device on post-operative pain and opioid use following anterior crucitate ligament reconstruction (ACLR), and thus residual opioids in circulation.

Being studied: VibraCool mechanical stimulation and neuromodulatory therapeutic device; Cryocompression (Game Ready, Bregs) device; Standard ice packs

Conditions: ACL; Opioid Use; Cryotherapy Effect; Vibration; Exposure; Pain, Postoperative

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Underwent ACL reconstruction

Exclusion Criteria

  • Pediatric iliotibial band ACL reconstruction (known to cause significantly more pain)
  • Non-english speakers (limitations of our study group)

Recruiting US locations

  • Columbia University Medical Center

    New York, NY 10032

    Site contact: Lauren H Redler, MD · 212-305-8188 · lr2505@cumc.columbia.edu

All healthy volunteers studies in New York →
VibraCool Device to Reduce Pain and Opioid Use After Anterior… (NCT06456268) | Bored Studies