Sevoflurane Sedation in Patients With Septic Shock

Shock, Septic Clinical Trial

— SSiS  

Official title:

Sevoflurane Sedation: A Potentially Promising Immunomodulation in Patients With Septic Shock

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03643367
• Other study ID #: SSiS
• Status: Not yet recruiting
• Phase: Phase 2
• Start date: January 2025
• Est. completion date: November 2025

Study information

• Verified date: December 2023
• Source: University of Zurich
• Contact: Martin Schlaepfer, PD
• Phone: +41 44 255 4690
• Email: martin.schlaepfer[@]usz.ch
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Description:

This randomized controlled trial (RCT) will be conducted over a period of 48 months, to investigate if volatile anesthetics have a positive effect on the prognostic sepsis marker IL-6. All patients with septic shock are intubated, ventilated and sedated with an intravenous anesthetic. In this study, eligible patients diagnosed with septic shock will be randomized 1:1 to the 'volatile group' with interruption of the propofol infusion, followed by a 4-hour sedation with the volatile anesthetic sevoflurane, or a continuous intravenous sedation ('intravenous' =control group). In both groups, 'intravenous' and 'volatile', the inflammatory markers as well as clinical parameters will be determined. The investigators will explore if there is a difference between the course of sepsis markers of the two groups within 5 days after intervention in favor of the volatile group.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 153
• Est. completion date: November 2025
• Est. primary completion date: February 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Male and female patients, age 18 to 80 years

• Intensive care Unit (ICU) patients with septic shock (despite fluid resuscitation vasopressors needed to maintain mean arterial pressure =65 millimeter of mercury (mmHg), and serum lactate >2mmol/l even with fluid application)

• Treatment of septic shock on ICU with vasopressors not longer than 12 hours

• Sedation and mechanical ventilation on ICU

• Female patients of childbearing potential with negative pregnancy test

• Informed Consent as documented by signature

Exclusion Criteria:

• Previous surgery and/or anesthesia (within last 7 days)

• Application of nitric oxide (NO)

• Suspected or known intolerance by history to volatile anesthetics (malignant hyperthermia)

• Immunosuppressive agents

• Systemic corticosteroids in the phase before hospitalization (> 10mg/d prednisone)

• Significant concomitant disease (acute cerebral vascular event, acute coronary syndrome, decompensated heart failure, acute pulmonary edema, major cardiac arrhythmia, seizure, burn, chronic kidney disease, end stage liver failure, neuromuscular disease)

• AIDS

• Autoimmune disease

• Organ transplant

• Subject with active malignancy receiving

• chemotherapy or radiation treatment within last 60 days

• Hepatitis B/C virus infection

• Anti-tumor necrosis factor (TNF) therapy

• Pregnancy and/or Breast feeding

• Use of cytokine absorber

• Enrollment in any other clinical trial during the course of this trial, 30 days prior to its beginning or 30 days after its completion

Related Conditions & MeSH terms

• Shock
• Shock, Septic

Intervention

Drug:
• Sevoflurane
Included patients, randomized in experimental group, intravenous sedation will be interrupted and followed by a 4 hour sedation with the volatile anesthetic sevoflurane.
• Control Group
Included patients randomized in control group, intravenouse sedation is continued with propofol

Locations

Country	Name	City	State
Switzerland	Kantonasspital Münsterlingen	Münsterlingen
Switzerland	University Hospital of Zurich	Zurich
Switzerland	Stadtspital Triemli	Zürich
Switzerland	Waidspital Zürich	Zürich

Sponsors (4)

Lead Sponsor	Collaborator
University of Zurich	Kantonsspital Münsterlingen, Triemli Hospital, Waid City Hospital, Zurich

Country where clinical trial is conducted

Switzerland, 

References & Publications (8)

Fleischmann C, Scherag A, Adhikari NK, Hartog CS, Tsaganos T, Schlattmann P, Angus DC, Reinhart K; International Forum of Acute Care Trialists. Assessment of Global Incidence and Mortality of Hospital-treated Sepsis. Current Estimates and Limitations. Am J Respir Crit Care Med. 2016 Feb 1;193(3):259-72. doi: 10.1164/rccm.201504-0781OC. — View Citation

Gordon AC, Mason AJ, Thirunavukkarasu N, Perkins GD, Cecconi M, Cepkova M, Pogson DG, Aya HD, Anjum A, Frazier GJ, Santhakumaran S, Ashby D, Brett SJ; VANISH Investigators. Effect of Early Vasopressin vs Norepinephrine on Kidney Failure in Patients With Septic Shock: The VANISH Randomized Clinical Trial. JAMA. 2016 Aug 2;316(5):509-18. doi: 10.1001/jama.2016.10485. — View Citation

Kellner P, Muller M, Piegeler T, Eugster P, Booy C, Schlapfer M, Beck-Schimmer B. Sevoflurane Abolishes Oxygenation Impairment in a Long-Term Rat Model of Acute Lung Injury. Anesth Analg. 2017 Jan;124(1):194-203. doi: 10.1213/ANE.0000000000001530. — View Citation

Klag T, Cantara G, Sechtem U, Athanasiadis A. Interleukin-6 Kinetics can be Useful for Early Treatment Monitoring of Severe Bacterial Sepsis and Septic Shock. Infect Dis Rep. 2016 Mar 21;8(1):6213. doi: 10.4081/idr.2016.6213. eCollection 2016 Mar 21. — View Citation

Lu Y, Wang J, Yan J, Yang Y, Sun Y, Huang Y, Hu R, Zhang Y, Jiang H. Sevoflurane attenuate hypoxia-induced VEGF level in tongue squamous cell carcinoma cell by upregulating the DNA methylation states of the promoter region. Biomed Pharmacother. 2015 Apr;71:139-45. doi: 10.1016/j.biopha.2015.02.032. Epub 2015 Mar 3. — View Citation

Rios-Toro JJ, Marquez-Coello M, Garcia-Alvarez JM, Martin-Aspas A, Rivera-Fernandez R, Saez de Benito A, Giron-Gonzalez JA. Soluble membrane receptors, interleukin 6, procalcitonin and C reactive protein as prognostic markers in patients with severe sepsis and septic shock. PLoS One. 2017 Apr 5;12(4):e0175254. doi: 10.1371/journal.pone.0175254. eCollection 2017. — View Citation

Tang BM, McLean AS, Dawes IW, Huang SJ, Lin RC. The use of gene-expression profiling to identify candidate genes in human sepsis. Am J Respir Crit Care Med. 2007 Oct 1;176(7):676-84. doi: 10.1164/rccm.200612-1819OC. Epub 2007 Jun 15. — View Citation

Tschaikowsky K, Hedwig-Geissing M, Braun GG, Radespiel-Troeger M. Predictive value of procalcitonin, interleukin-6, and C-reactive protein for survival in postoperative patients with severe sepsis. J Crit Care. 2011 Feb;26(1):54-64. doi: 10.1016/j.jcrc.2010.04.011. Epub 2010 Jun 19. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Concentration of interleukin-6 over time	To see if the interleukin-6 decreases under the influence of sevoflurane	5 days
Secondary	Pro-/anti-inflammatory mediators	effect on inflammatory/anti- inflammatory mediators	5 days
Secondary	Vasopressor support	Use of vasopressor support (norepinephrine, dobutamine, vasopressin) will be determined.	5 days
Secondary	Sequential organ failure score (SOFA Score)	Sepsis related organ failure score	5 days
Secondary	Richmond Agitation Sedation Scale	A scale to measure the agitation or sedation level of a patient	5 days
Secondary	Duration of mechanical ventilation	Time of mechanical ventilation	28 days
Secondary	Mortality	Mortality information in intensive care unit and on the ward	28 days