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NOT YET RECRUITING
NCT07612579

PROSEVO Trial (Propofol-Sevoflurane Delirium Target Trial Emulation)

Sponsor: Charite University, Berlin, Germany

View on ClinicalTrials.gov

Summary

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 Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

100000

Start Date

2026-05-26

Completion Date

2027-12

Last Updated

2026-05-28

Healthy Volunteers

Not specified

Locations (2)

Department of Anesthesiology and Intensive Care Medicine (CBF), Charité - Universitätsmedizin Berlin

Berlin, Germany

Department of Anesthesiology and Intensive Care Medicine Berlin

Berlin, Germany