Pumping chemo straight into the liver: a new way to fight pancreatic cancer spread?
NCT ID NCT07845617
First seen Sep 29, 2026 · Last updated Sep 30, 2026 · Updated 1 time
Summary
This study looks at whether delivering chemotherapy directly into the liver through a small implanted pump can help people with pancreatic or duodenal adenocarcinoma that has spread to the liver after surgery and standard chemotherapy. Participants receive floxuridine through the pump and researchers track tumor response on scans, progression-free survival, overall survival, and complications from the pump or procedure. The study is small, with about 10 participants, and aims to see if this approach is feasible and worth testing further.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- floxuridine (FUDR) chemotherapy delivered through a hepatic artery infusion pump
- What this could lead to
- If it works, this approach could offer a way to control cancer that has spread to the liver in people whose pancreatic or duodenal cancer was already treated with surgery and chemotherapy.
- What could go wrong
- The study is very small, with only 10 participants, and it is a feasibility study, so it mainly checks whether the approach can be done and monitored, not whether it clearly extends life. Pump placement and liver-directed chemotherapy carry risks of surgical complications, catheter problems, and liver toxicity.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 10 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Nov 2026
An estimate. Start dates often move.
- Expected to finish
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May 2028
An estimate. End dates often move.
- 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.
Who is studied
AdventHealth Orlando
- Ages
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18 to 80 years
- 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 18-80 years * Histologically confirmed pancreatic or duodenal adenocarcinoma * Completed or currently receiving curative-intent treatment * Evidence of isolated or liver-dominant metastases (radiographic or clinical) * Deemed clinically eligible for hepatic artery infusion pump (HAIP) placement and floxuridine (FUDR)-based chemotherapy by a multidisciplinary oncology team * Scheduled for HAIP placement at AdventHealth Orlando Exclusion Criteria: \- Patients who are clinically ineligible for HAIP placement or FUDR therapy are excluded
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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AdventHealth Orlando
RECRUITINGOrlando, Florida, 32804, United States
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