Can a targeted nerve block outsmart pancreatic cancer pain?
NCT ID NCT00974948
First seen Aug 14, 2026 · Last updated Aug 14, 2026
Summary
This trial tests whether an ultrasound-guided injection of alcohol and a numbing agent around the celiac ganglia can relieve pain in people newly diagnosed with inoperable pancreatic cancer. Participants receive either the nerve block or a sham procedure, alongside standard pain management. The study compares pain scores, opioid use, quality of life, and survival over three months to see if early nerve destruction can prevent pain from escalating.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- EUS-guided celiac plexus neurolysis (injection of alcohol and bupivacaine around the celiac ganglia)
- What this could lead to
- If effective, this procedure could offer a new way to control pain early in pancreatic cancer, potentially reducing the need for strong narcotics and improving quality of life.
- What could go wrong
- The procedure is invasive and carries risks like bleeding or nerve damage. It may not provide better pain relief than standard narcotics, and the trial is still in phase 3, so results are not yet confirmed.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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100 people
The number who actually took part.
- Start date
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Apr 2006
- Finished
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Dec 2008
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * previous imaging and/or the EUS examination demonstrated inoperable pancreatic cancer defined as involvement of the superior mesenteric vein, portal vein or confluence, superior mesenteric artery, celiac axis, hepatic artery, or non-regional lymphadenopathy * a new diagnosis of pancreatic adenocarcinoma was confirmed by an on-site cytopathologist following EUS fine needle aspiration (EUS-FNA) Exclusion Criteria: * allergy to bupivicaine * possible future surgical management of the tumor * expected survival less than 3months (suspected or proven carcinomatosis or liver metastases) * inability or unwillingness to provide informed consent prior to the EUS
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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CHUM
Montreal, Quebec, H2X 3J4, Canada