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.
Clinical Trial of Endoscopically Guided Injection of Exparel (Bupivacaine) for the Treatment of Craniofacial Pain
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Peter Hwang, MD · PRINCIPAL_INVESTIGATOR · Stanford University
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
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.
Inclusion
Exclusion
What this trial measures
- Change of Pain ScoreBaseline to day 21
Scores range from 0-10 (0=no pain, 10=worst pain)