Massive new study aims to stop Post-Surgery confusion in seniors
NCT ID NCT04355195
First seen Jun 27, 2026 · Last updated Sep 01, 2026 · Updated 4 times
Summary
This study tests a structured care program to prevent postoperative delirium (sudden confusion) in patients aged 70 and older undergoing surgery. Over 18,000 participants will receive evidence-based prevention measures, with electronic tracking to ensure consistency. Additional sub-studies explore how blood pressure changes and brain wave monitoring might predict delirium risk.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- structured care program (evidence-based prevention measures, electronic documentation, and monitoring devices)
- What this could lead to
- If successful, this could establish a practical, hospital-wide approach to reduce postoperative delirium in older patients, improving recovery and quality of life.
- What could go wrong
- This is an implementation study, not a drug trial, so benefits depend on hospital staff following the program consistently. The sub-studies are exploratory and may not yield clear results.
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 18,100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2020
- Expected to finish
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Jun 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
Patients aged ≥70 years, male and female, who are receiving surgery
- Ages
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70 years and older
- Sex
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Anyone
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: * Age ≥ 70 years * male and female patients * Patients who are insured with BARMER, HEK, KKH, DAK, TK or hkk Health insurances * Patients eligible for inclusion: by the patient, preoperatively * Incapacitated patients for inclusion: Written informed consent by a legal representative * surgery (elective and not elective) Exclusion criteria: * Moribund patients * Not enough language skills
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Department of Anesthesiology and Intensive Care Medicine (CBF), Charité - Universitätsmedizin Berlin
RECRUITINGBerlin, 12203, Germany
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Department of Anesthesiology and Intensive Care Medicine (CCM/CVK) Berlin, Carité - Universitätsmedizin Berlin
RECRUITINGBerlin, 13353, Germany
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- A new care routine aims to shield aging hearts and minds in the ICU
- Bedrest be gone? gamified therapy aims to keep seniors moving in the hospital
- Which alarm keeps delirious patients safer? new study tests two High-Tech solutions
- Tiny study compares trazodone and quetiapine for ICU delirium – but was cut short
- New study aims to stop Post-Surgery confusion with sleep and brain training
- Simple signs and amplifiers may cut hospital delirium