Can a palliative care team boost quality of life for cancer surgery patients?
NCT ID NCT03611309
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at whether having a palliative care team work alongside surgeons improves quality of life for patients with gastrointestinal cancers like pancreatic or liver cancer. About 379 patients and their family members took part. The main goal was to see if this team approach leads to better well-being 12 weeks after surgery compared to standard surgeon-only care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- palliative care team co-management
- What this could lead to
- If successful, this approach could improve quality of life and emotional well-being for patients and families facing major cancer surgery.
- What could go wrong
- This is a completed trial, but the intervention is supportive care, not a cure. Benefits may be modest and not apply to all cancer types or settings.
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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379 people
The number who actually took part.
- Started
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Sep 2018
- Finished
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Aug 2022
- 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: * 18 years of age and must be able to give informed consent. * Diagnosed with pancreatic cancer or hepatocellular cancer or esophageal cancer or gastric cancer and/or cholangio carcinomas * Non emergent, upper gastrointestinal cancer related surgery with a goal of primary resection of the tumor- optimal surgical goal is cure, not merely disease palliation. * One companion per patient will be allowed to participate. In addition, to being identified by the patient at being a key caregiver throughout the surgery period, these companions must be able to give informed consent and at least 18 years of age. Exclusion Criteria: * No previous involvement of palliative care providers in their care course
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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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Dana Farber/ Brigham
Boston, Massachusetts, 02115, United States
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Johns Hopkins Hostpital
Baltimore, Maryland, 21287, United States
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Ohio State University Medical Center
Columbus, Ohio, 43210, United States
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Stanford University
Stanford, California, 94304, United States
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University of New Mexico
Albuquerque, New Mexico, 87131, United States
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