Clinical Trial

Sevoflurane Sedation in Patients With Septic Shock

Study acronym: SSiS
Not Yet Recruiting Phase 2
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Summary
Recent in vivo studies from others as well as the investigators group demonstrated that volatile anesthetics immunomodulate sepsis and improve outcome. Also, several clinical trials have convincingly shown that application of a volatile anesthetic provides protection in patients undergoing major surgery. Patients with sepsis are intubated and ventilated and therefore need sedation. So far, most ICU centers use intravenously applied sedatives in these patients. In the proposed study, we will switch sedation from an intravenous to a volatile anesthetic for a short period of time to explore if sepsis markers improve within the following 120 hours upon sevoflurane conditioning.
Protocol Amendment History 5 amendments
This ClinicalTrials.gov record has been amended 5 times since 2018-08-21; most recent amendment 2025-03-26.
Trial Details
NCT Number NCT03643367
Lead Sponsor University of Zurich
Collaborators: Kantonsspital Münsterlingen, Triemli Hospital, Waid City Hospital, Zurich
Conditions Shock, Septic
Enrollment 153 participants
Start Date 2026-01
Primary Completion 2027-02 (estimated)
Study Completion 2027-11 (estimated)
Updated on ClinicalTrials.gov 2025-04-01