Can big data unlock the secrets to safer surgery?
NCT ID NCT05560815
First seen Aug 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time
Summary
This study analyzes data from over a million adults who had surgery in Sweden between 2015 and 2020. It aims to identify which patient, anesthesia, and surgical factors are linked to better or worse outcomes, such as survival and complications. By examining the entire perioperative process, the researchers hope to find ways to improve care and reduce suffering.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could identify ways to better predict and improve surgical outcomes, leading to safer, more effective perioperative care.
- What could go wrong
- This is an observational study, so it cannot prove cause and effect. Results may be influenced by unmeasured factors and may not apply outside Sweden.
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.
- Participants
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About 1,500,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2022
- Expected to finish
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Dec 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.
Who is studied
All adult (≥18 years) patients that have undergone any type of surgical procedure during 1 Jan 2015 - 31 Dec 2020 and are registered in the Swedish Perioperative Registry (SPOR).
- 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: * Underwent any surgical procedure in Sweden during the time period 1 Jan 2015 - 31 Dec 2020 * Registered in the Swedish Perioperative Registry (SPOR) * ≥18 years of age * Swedish social security number (to enable follow-up) Exclusion Criteria: * incorrect social security number * incomplete mortality data * the patient has chosen to opt-out of the register The first two exclusion criteria are applied because they prevent correct follow-up of the primary outcome measure (mortality)
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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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Department of Anaesthesia and Intensive Care, Linkoeping University Hospital
Linköping, Östergötland County, 50185, Sweden
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Other studies related to the condition(s) this trial covers.
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- Can a scented spray soothe Post-Surgery throat pain and nausea?
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