Heat therapy gives new hope for advanced pancreatic cancer patients
NCT ID NCT07191418
First seen Jun 27, 2026 · Last updated Aug 25, 2026 · Updated 2 times
Summary
This study tests whether adding a heat-based treatment called radiofrequency ablation (RFA) to a standard procedure (ERCP) can help people with advanced pancreatic cancer that has spread to the liver live longer. About 178 adults with limited liver spread will be randomly assigned to get either the standard ERCP alone or ERCP plus RFA. The goal is to see if the added heat treatment improves cancer-specific survival.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 178 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2026
- Expected to finish
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Sep 2027
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
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 to 85 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.
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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: * Individuals with newly diagnosed pancreatic cancer in the head of the pancreas causing compression on the bile duct. * Metastatic stage to the liver * Histologically or cytologically confirmed mPDAC. * Cancer burden limited to maximum 5 metastases in the liver, each of them maximum 1 cm in the larger diameter. * Patients must be under palliative chemotherapy treatment. * Cancer should be radiologically measurable (in an area not previously irradiated). * WHO performance status 0-2. * Age 18-85 years. Exclusion Criteria: * Intellectual disability, unwillingness or language difficulties * which hinders the ability to give informed consent. * Ongoing extensive immunosuppression and/or severe leuko- or * thrombocytopenia. * Ongoing acute cholangitis. * Ongoing sepsis. * Acute kidney failure. * Uncompensated heart failure or unstable coronary insufficiency * (symptomatic/uncompensated). * Pregnancy or breastfeeding. * Any metastases outside the liver. * Cardiac pacemakers/cardioverter defibrillators. * Severe coagulopathy.
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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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Department of Surgery, Umeå University Hospital
RECRUITINGUmeå, 90185, Sweden
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