NCT06737237

Cervical Plexus Versus Infiltration for Clavicular Operations (CERPICO)

Enrolling by Invitation
NAAges 18–64InterventionalTreatment
Naval Medical Center Camp Lejeune
~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
Clavicle Surgery
Clavicle Fracture
Acromioclavicular Joint
Coracoclavicular Ligament

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.

  • CDR Lee, MD · PRINCIPAL_INVESTIGATOR · DHA/MD365

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
  • 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