Cancer surgery recovery: quality of life under the microscope
NCT ID NCT04444544
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tracked 295 adults who had high-risk surgery for stomach, esophagus, pancreas, or liver cancer. Researchers measured quality of life before surgery and again at 6 and 12 months after. They also asked patients and their family members if they regretted the decision to have surgery. The goal was to understand patterns of improvement, stability, or decline in well-being after these major operations.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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295 people
The number who actually took part.
- Started
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Sep 2020
- Finished
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Jul 2025
- 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
Elective patients scheduled for high-risk abdominal cancer surgery
- 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.
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: \- Adult patients (\>18 years) scheduled for the following elective abdominal cancer surgery known for high one-year mortality4: gastrectomy; esophagectomy; pancreas resection and hepatectomy Exclusion Criteria: * Patients with inoperable tumours; i.e. some patients will be excluded at the time of surgery if unexpected advanced tumour staging is confirmed intraoperatively (e.g. peritoneal carcinomatosis or any other diagnosis without therapy). * Hepatectomy for metastasectomy * Mentally impaired patients (known diagnosis) * Psychotic diagnoses (i.e. schizophrenia) * Dementia (mini mental score (MMSE) \< 18) * Incapacity to understand the information sheet * Blindness (unable to perform the visual part of the mini-mental state examination)
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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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University Hospitals of Geneva
Geneva, 1206, Switzerland
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