PROSEVO Trial (Propofol-Sevoflurane Delirium Target Trial Emulation)

Recruiting now

Conditions studied: Postoperative Delirium

In brief

The results of this study have significant implications for clinical practice and guideline development. The current European guideline on postoperative Delirium prevention (ESAIC 2024) explicitly identifies a lack of large, adequately powered studies comparing different anesthetic techniques and is therefore currently unable to provide clear recommendations on the selection of an optimal technique. This study will close this knowledge gap and thus support future guideline recommendations. The results could show that a particular anesthetic technique (e.g., propofol) is associated with a significantly lower risk of postoperative delirium; if so, this would have immediate implications for modifying standard anesthesia protocols in hospitals. Furthermore, Delirium is a significant public health challenge in aging societies. With demographic aging, the number of older patients undergoing surgery is continuously increasing. The societal costs of Delirium are estimated at several billion euros per year in major industrialized nations. A reduction in the incidence of postoperative Delirium by just 10% through optimization of the anesthetic procedure would therefore have major health economic implications.

Key facts

Study ID

NCT07612579

Run by

Charite University, Berlin, Germany

People needed

100000

Starts

2026-06-03

Expected to finish

2027-12-01

Last updated by the study team

2026-06-04

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adult patients (≥18 years) at the Department of Anesthesiology and Intensive Care Medicine (CCM/CVK) and the Department of Anesthesiology and Intensive Care Medicine (CBF) at Charité,
• undergoing elective surgery under general anesthesia
• with a planned surgery duration of ≥ 30 minutes
• In addition, the following conditions must be met:
• The surgery must be the patient's first surgery per hospital stay to avoid dependencies and repeated measurements of the same person within a short time frame;
• The surgeries take place at Charité between January 1, 2011, and December 31, 2025.

You may not qualify if…

• Patients in any of the following situations are excluded:
• Cardiac surgery (this patient group requires specialized monitoring strategies and has postoperative delirium risk profiles that differ significantly from those of other types of surgery)
• preoperatively diagnosed delirium, defined as positive results on the Nursing Delirium Screening Scale (NU-DESC) or the Confusion Assessment Method for the Intensive Care Unit (CAM-ICU) during preoperative evaluations;
• severe preoperative cognitive impairment, defined as a Mini-Mental State Examination (MMSE) score <15 points, or
• preoperatively documented severe dementia
• neurosurgical procedures (neurosurgical patients require specialized monitoring protocols and differ from other surgical patients in their postoperative delirium (POD) symptoms)
• Patients who were already admitted to intensive care units prior to their elective surgery (these patients already have increased mortality and a different risk profile)
• Patients who were already intubated or sedated prior to surgery (this group cannot undergo standardized POD screening)
• High preoperative risk for postoperative nausea and vomiting (PONV) (specifically, patients with documented PONV grade 3 or PONV grade 4 risk are excluded, as this group is indicated for anesthesia with propofol)

Where it is running

• Department of Anesthesiology and Intensive Care Medicine (CBF), Charité - Universitätsmedizin Berlin — Berlin, Germany (enrolling)
• Department of Anesthesiology and Intensive Care Medicine Berlin — Berlin, Germany (enrolling)

Full record on ClinicalTrials.gov

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