Can early comfort care boost quality of life in pancreatic cancer?
NCT ID NCT04632303
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tests whether starting palliative care early—right after diagnosis—improves quality of life for people with advanced pancreatic cancer. 250 participants receive regular visits from a palliative care team, plus referrals to exercise and nutrition experts. The goal is to see if this approach helps patients feel better and possibly live longer.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Early palliative care (specialist visits, exercise referral, nutritional support)
- What this could lead to
- If it works, this could show that starting palliative care early helps people with advanced pancreatic cancer feel better and live better.
- What could go wrong
- This is a supportive care study, not a treatment for the cancer itself. It may not improve survival or quality of life for everyone.
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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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 250 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2021
- Expected to finish
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Nov 2026
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.
- 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: * Adult males and females (aged 18 and over) * Confirmed by cytology or histology incurable PDAC who are planned to receive medical care for cancer in the first-line setting at the enrolling institution within ≤ 2 weeks * Written informed consent before any study procedures * Performance status: ECOG 0-2 * Ability to read and respond to questions or able to complete questions with minimal assistance required from an interpreter or family member * Planning to receive all medical care for cancer at the enrolling institution. Exclusion Criteria: * Patients who are already receiving care from the palliative care service are not eligible for participation in the study * Exhibiting signs of overt psychopathology or cognitive dysfunction * Any medical condition that the Investigator considers significant to compromise the safety of the patient or that impairs the interpretation of study assessments * Patient participating in another interventional study during the surveillance period. This is only relevant for studies that might interfere with the intervention. Participation in protocols related only to treatment will not preclude participation in the present study. Cases of doubt will be settled by the protocol responsible.
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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
-
Herlev & Gentofte University Hospital, Denmark
Herlev, 2730, Denmark
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