NCT06737237
Cervical Plexus Versus Infiltration for Clavicular Operations (CERPICO)
Enrolling by Invitation
NAAges 18–64InterventionalTreatmentNaval Medical Center Camp LejeuneGovernment-funded
~40 participants
Updated 2026-04-16 on ClinicalTrials.gov
What's tested:cervical plexus blockLocal Infiltration Analgesia (LIA)
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Total Perioperative Intravenous Fentanyl Administration
Measured over from anesthesia start time to discharge from PACU, estimated 3-4 hours
Conditions
Where it's being run
1 sites across 1 statesNorth Carolina1
Study leadership
- CDR Lee, MD · PRINCIPAL_INVESTIGATOR · DHA/MD365
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Eligibility criteria
Inclusion
Adults aged 18-64 years
Scheduled surgery of the clavicle, acromioclavicular joint, or coracoclavicular ligament at NMCL
ASA Physical Status Classification 1-3
Exclusion
Emergent surgery
Concurrent surgery involving the glenobumeral joint or proximal humerus
Prior anaphylactic reaction or known intolerance to study medications
Patient reported or documented opioid use within the last 30 days unrelated to clavicular, AC joint, or CC ligament pathology
What this trial measures
- Total Perioperative Intravenous Fentanyl Administrationfrom anesthesia start time to discharge from PACU, estimated 3-4 hours
total fentanyl dosage (mcg) encompassing the intraoperative and PACU recovery periods