Clinical Trial of Exparel for Craniofacial Pain

This study is testing if an injection of Exparel (bupivacaine), a non-opioid pain reliever, can help people with craniofacial pain, including migraines, cluster headaches, and other severe head pains. Researchers will inject Exparel or a saline placebo into the side of the nose using a special camera (endoscope). The goal is to see if Exparel can reduce your pain score over 21 days. You may be able to join if you are 18-80 years old, have craniofacial pain, and have had a visit to the Stanford Pain & ENT clinic. The study is currently unclear on its recruitment status and plans to enroll 15 participants.

Study design
This is a randomized, double-blinded, placebo-controlled, and cross-over study involving about 15 participants. This means you will randomly receive either Exparel or a placebo, and neither you nor your doctor will know which you received.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Your pain score will be measured from the start of the study until day 21.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT04930887

Clinical Trial of Endoscopically Guided Injection of Exparel (Bupivacaine) for the Treatment of Craniofacial Pain

Recruiting
PHASE2Ages 18–80InterventionalTreatment
Stanford University
~15 participants
Updated 2026-04-27 on ClinicalTrials.gov
What's tested:Exparel (Bupivacaine Liposome)Saline

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Change of Pain Score
Measured over Baseline to day 21
Craniofacial Pain
Migraine
Cluster Headache
Trigeminal Autonomic Cephalgia
Sphenopalatine Ganglion Neuralgia
Paroxysmal Hemicrania
1 sites across 1 states
California1
  • Peter Hwang, MD · PRINCIPAL_INVESTIGATOR · Stanford University

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Patients with a chief complaint of craniofacial pain (migraine, cluster headache, trigeminal autonomic cephalgia, sphenopalatine ganglioneuraligia, paroxysmal hemicrania) who has Stanford Pain \& ENT clinic visit

Exclusion

age \<18 or \>80
pregnant women
economically disadvantaged (not able to afford clinic visits/treatments)
decisionally impaired (unable to obtain informed consent)
has allergy to bupivacaine
unable or unwilling to participate plans to participate in another clinical study at any time during this study
  • Change of Pain ScoreBaseline to day 21

    Scores range from 0-10 (0=no pain, 10=worst pain)