Your genes may hold the key to predicting Post-Surgical pain
NCT ID NCT02383342
First seen Aug 12, 2026 · Last updated Aug 13, 2026 · Updated 1 time
Summary
This study aims to find out whether a person's genes and clinical profile can predict who will develop acute or chronic pain after major surgery. Researchers will follow 10,000 patients for one year after their operation, tracking pain levels and daily functioning. The goal is to identify biomarkers that could help doctors personalize pain treatment early, potentially preventing long-term 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 lead to a simple test or checklist to predict a patient's risk of chronic pain after surgery, allowing doctors to personalize pain treatment early.
- What could go wrong
- This is an observational study, so it cannot prove cause and effect. The genetic findings may be complex and require years of further research before they can be used in everyday care.
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 10,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2015
- Expected to finish
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Mar 2029
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.
Who is studied
All adult patients undergoing elective major surgery at Radboud university medical center (Nijmegen, The Netherlands) Patients will be recruited prospectively and consecutively via the anaesthetic preoperative outpatients' clinic.
- Ages
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18 to 80 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.
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: Patients: * Ages 18 - 80 years, consenting, planned surgery, able to understand and answer questionnaires. Exclusion Criteria: * Non-consent, inability to give consent, unplanned and emergency surgery.
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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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Radboudumc
Nijmegen, 6500HB, Netherlands
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Other studies related to the condition(s) this trial covers.
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