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
NCT06737237
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Naval Medical Center Camp Lejeune
Marine Corps Base Camp Lejeune, North Carolinano site contact published
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- CDR Lee, MD · PRINCIPAL_INVESTIGATOR · DHA/MD365
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
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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