EUS-guided Celiac Plexus Block for Chronic Pancreatitis Pain
This study is looking at whether a procedure called EUS-guided celiac plexus block can help reduce abdominal pain in people with chronic pancreatitis. During this procedure, a doctor uses an endoscope (a thin, flexible tube with a camera) and ultrasound to guide an injection of bupivacaine (a local anesthetic) and triamcinolone (a steroid) near the celiac plexus nerves in your abdomen. Some participants will receive this injection, while others will have a sham procedure where no injection is given. The study aims to enroll 94 participants and is currently unclear if it's recruiting. To join, you must be at least 18 years old, have had abdominal pain for at least 3 months with a pain score of 3 or higher, and have a diagnosis of chronic pancreatitis based on specific EUS findings. The main goal is to see if participants experience adequate pain relief after one month.
- Study design
- This is an interventional study comparing EUS-guided celiac plexus block to a sham procedure. It plans to enroll 94 participants.
- What's involved
- Participants will undergo either an EUS-guided celiac plexus block or a sham procedure.
- Compensation
- Not stated in the trial record.
- Follow-up
- Pain relief will be measured at 1 month after the procedure.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
EUS-guided Celiac Plexus Block vs. Sham in Chronic Pancreatitis
At a glance
Conditions
Where it's being run
1 sites across 1 statesWho 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
- Rate of adequate pain relief1 month
Rate of adequate pain relief in patients with chronic pancreatitis undergoing endoscopic ultrasound-guided celiac plexus block or sham procedure. Adequate pain relief is defined as a 50% reduction in composite pain score from baseline, measured using the Brief Pain Inventory-Short Form, at 1 month post-intervention.