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Esmolol Effects on Heart and Inflammation in Septic Shock (ESMOSEPSIS)

Primary Purpose

Septic Shock

Status
Unknown status
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Esmolol
Sponsored by
Central Hospital, Nancy, France
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Septic Shock focused on measuring Septic Shock, Hemodynamic, Inflammatory status, Beta adrenergic modulation, Esmolol

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • septic shock patients following the definition of the Surviving Sepsis Campaign
  • femoral and central venous catheters for thermodilution monitoring
  • fluid optimization
  • with a cardiac index > 3 l/min/m2
  • Heart Rate >100 /min

Exclusion Criteria:

  • Cardiogenic shock
  • Bradycardia
  • History of Severe Asthma
  • Indications against esmolol

Sites / Locations

  • CHU de NancyRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

ESMOLOL

Arm Description

Resuscitated, hyperkinetic septic shock patients are treated with esmolol in order to reduce heart rate of 20% during 6 hours. During the intervention period, multimodal macro and micro hemodynamic data are recorded.

Outcomes

Primary Outcome Measures

Hemodynamic effects of Esmolol in septic shock patients (Value of cardiac index l/min/m2)
Compare, in septic shock patients, the mean cardiac index before and after administration of Esmolol.

Secondary Outcome Measures

Effects on vasopressor requirement (amount of norepinephrine infused in microgram/kg) during Esmolol administration
Microcirculatory and regional circulation effects of Esmolol in septic shock patient
NIRS (near-infrared spectroscopy) SDF (Sidestream Dark Field imaging) / Limon (non-invasive measurement of liver function and splanchnic perfusion monitoring) are used to asses microcirculatory and regional circulation effects
Changes in the Cytokine pattern(pro and anti inflammatory cytokines assay) induced by Esmolol administration in septic shock patients
Description of the cardiac function during Esmolol Administration in septic shock patients
Use of Echocardiography to assess ventricular function

Full Information

First Posted
January 29, 2014
Last Updated
January 27, 2016
Sponsor
Central Hospital, Nancy, France
Collaborators
Baxter Healthcare Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT02068287
Brief Title
Esmolol Effects on Heart and Inflammation in Septic Shock
Acronym
ESMOSEPSIS
Official Title
Anti-inflammatory and Cardiac Effects of Esmolol in Septic Shock. ESMOSEPSIS Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2016
Overall Recruitment Status
Unknown status
Study Start Date
December 2013 (undefined)
Primary Completion Date
December 2016 (Anticipated)
Study Completion Date
June 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Central Hospital, Nancy, France
Collaborators
Baxter Healthcare Corporation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Beta adrenergic system, over-activated in septic shock patients, is a key modulator of the inflammatory response. Experimental works demonstrated that Esmolol, an highly selective beta-1 blocker, reduces heart rate and regulates the inflammatory response. A recent mono centric, double blind, randomized clinical work in septic shock patients has shown that Esmolol administration is safe and reduces effectively heart rate. However there are only sparse data on 1) regional and micro-circulation, 2) inflammation modulation in human resuscitated septic shock patients treated by esmolol.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Septic Shock
Keywords
Septic Shock, Hemodynamic, Inflammatory status, Beta adrenergic modulation, Esmolol

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
25 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ESMOLOL
Arm Type
Experimental
Arm Description
Resuscitated, hyperkinetic septic shock patients are treated with esmolol in order to reduce heart rate of 20% during 6 hours. During the intervention period, multimodal macro and micro hemodynamic data are recorded.
Intervention Type
Drug
Intervention Name(s)
Esmolol
Other Intervention Name(s)
Brevibloc
Intervention Description
After, at least six hours of hemodynamic optimization, patients with an hyper dynamic shock received a conventional management with a continuous infusion of Esmolol titrated to gain a 20% reduction in heart rate. This infusion is maintained for six hours.
Primary Outcome Measure Information:
Title
Hemodynamic effects of Esmolol in septic shock patients (Value of cardiac index l/min/m2)
Description
Compare, in septic shock patients, the mean cardiac index before and after administration of Esmolol.
Time Frame
Before administration (H0) and each hour (H1-H2-H3-H4-H5-H6) during the whole administration period and one hour after Esmolol cessation (H7)
Secondary Outcome Measure Information:
Title
Effects on vasopressor requirement (amount of norepinephrine infused in microgram/kg) during Esmolol administration
Time Frame
Record of each change in vasopressor dosage to maintain a mean arterial pressure at 70 mmHg during the whole Esmolol administration period (H0 to H6) and one hour after esmolol cessation (H7)
Title
Microcirculatory and regional circulation effects of Esmolol in septic shock patient
Description
NIRS (near-infrared spectroscopy) SDF (Sidestream Dark Field imaging) / Limon (non-invasive measurement of liver function and splanchnic perfusion monitoring) are used to asses microcirculatory and regional circulation effects
Time Frame
Before (H0), 6 hours after Esmolol introduction (H6) and 1 hour after esmolol cessation (H7)
Title
Changes in the Cytokine pattern(pro and anti inflammatory cytokines assay) induced by Esmolol administration in septic shock patients
Time Frame
Before administration of Esmolol (H0) and 6 hours after introduction of Esmolol (H6)
Title
Description of the cardiac function during Esmolol Administration in septic shock patients
Description
Use of Echocardiography to assess ventricular function
Time Frame
Before administration (H0), at 4 hours, 6 hours after introduction and 1 hours after esmolol cessation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: septic shock patients following the definition of the Surviving Sepsis Campaign femoral and central venous catheters for thermodilution monitoring fluid optimization with a cardiac index > 3 l/min/m2 Heart Rate >100 /min Exclusion Criteria: Cardiogenic shock Bradycardia History of Severe Asthma Indications against esmolol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bruno Levy, MD PhD
Organizational Affiliation
CHU de Nancy
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Antoine Kimmoun, MD
Organizational Affiliation
CHU de Nancy
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU de Nancy
City
Nancy
ZIP/Postal Code
54511
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bruno Levy, MD PhD
Phone
0033383154469
Email
b.levy@chu-nancy.fr

12. IPD Sharing Statement

Citations:
PubMed Identifier
33413583
Citation
Levy B, Fritz C, Piona C, Duarte K, Morelli A, Guerci P, Kimmoun A, Girerd N. Hemodynamic and anti-inflammatory effects of early esmolol use in hyperkinetic septic shock: a pilot study. Crit Care. 2021 Jan 7;25(1):21. doi: 10.1186/s13054-020-03445-w.
Results Reference
derived

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Esmolol Effects on Heart and Inflammation in Septic Shock

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