VibraCool Device to Reduce Pain and Opioid Use After Anterior Cruciate Ligament Reconstruction (ACLR)
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorColumbia University
About this trial
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.
Eligibility criteria
Qualifiers
Underwent ACL reconstruction
Disqualifiers
Pediatric iliotibial band ACL reconstruction (known to cause significantly more pain)
Non-english speakers (limitations of our study group)
Trial design
Treatments tested in this trial
- VibraCool mechanical stimulation and neuromodulatory therapeutic device
- Cryocompression (Game Ready, Bregs) device
- Standard ice packs
Treatment groups
130 Participants
are divided into 3 treatment groupsLocations
1Columbia University Medical Center10032, New YorkNew York, United States
Sponsors and collaborators
Columbia University
Lead sponsor
Source ClinicalTrials.gov