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Transpulmonary Thermodilution and Transesophageal Echocardiography in Early Septic Shock (HEMOSEPSIS)

Primary Purpose

Septic Shock

Status
Completed
Phase
Phase 4
Locations
France
Study Type
Interventional
Intervention
early septic shock
Sponsored by
University Hospital, Limoges
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Septic Shock

Eligibility Criteria

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

Inclusion Criteria:

  • ventilated patient in sinus rhythm with septic shock requiring a hemodynamic assessment

Exclusion Criteria:

  • < 18 yr-old
  • pregnancy
  • contra-indication for TEE, non sinus rhythm, aplasia, prior participation to the study, hemodynamic assessment using any other technique than those tested in the study.

Sites / Locations

  • Bordeaux UH
  • Toulouse UH

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

septic shock TPT then TEE

septic shock TEE then TPT

Arm Description

Group 1: Each patient will be assessed by both the transpulmonary thermodilution technique and transesophageal echocardiography (TEE)..

Goup 2: Each patient will be assessed by both transesophageal echocardiography (TEE) and the transpulmonary thermodilution technique.

Outcomes

Primary Outcome Measures

therapeutic procedure following the hemodynamic assessment
Changes in therapy proposed after the hemodynamic assessment (hemodynamic profile) by each of the two tested methods: blood volume expansion (preload responsiveness), positive inotrope (cardiac dysfunction), vasopressor (vasoplegia), no change in ongoing therapy or dose tapering (inotropes or vasopressor).

Secondary Outcome Measures

efficacy and safety of therapeutic intervention
Efficacy (clinical problem solved) and tolerance (potential side-effects) of the therapeutic change.

Full Information

First Posted
August 25, 2010
Last Updated
August 20, 2018
Sponsor
University Hospital, Limoges
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1. Study Identification

Unique Protocol Identification Number
NCT01188993
Brief Title
Transpulmonary Thermodilution and Transesophageal Echocardiography in Early Septic Shock
Acronym
HEMOSEPSIS
Official Title
Hemodynamic Assessment With Transpulmonary Thermodilution and Transesophageal Echocardiography in Patients With Early Septic Shock
Study Type
Interventional

2. Study Status

Record Verification Date
August 2010
Overall Recruitment Status
Completed
Study Start Date
January 2011 (undefined)
Primary Completion Date
January 2014 (Actual)
Study Completion Date
December 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Limoges

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to assess the concordance of therapeutic changes proposed after an early hemodynamic evaluation (hemodynamic profile) in septic shock patients using jointly the transpulmonary thermodilution technique and transesophageal echocardiography (TEE).
Detailed Description
Each patient will be assessed by both the transpulmonary thermodilution technique and TEE (H0). The two assessments will be performed in random order (central randomization stratified by participating center), but within 30 minutes (no change of ongoing treatment during the assessment period). Two investigators not involved in patient care and blinded to the results of the alternative technique will performed independently the hemodynamic assessment using one of the two modalities for hemodynamic assessment tested in the study. They will interpret the results at bedside and propose a therapeutic change to the attending physician, according to the hemodynamic profile. The latter will finally: precisely identify the clinical problem to be solved (e.g., therapeutic target of the Surviving Sepsis Campaign not reached, tissue hypoperfusion), choose a therapy adapted while taking into account the clinical scenario and the results of both the transpulmonary thermodilution and TEE, evaluate the efficacy of this treatment (problem solved or not) and its tolerance (potential side-effect attributable to the treatment). In addition, the presence or resolution of signs of tissue hypoperfusion will systematically be assessed at H6, H12 and H24. Primary and secondary outcomes will be assessed by an independent committee of experts.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Septic Shock

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
153 (Actual)

8. Arms, Groups, and Interventions

Arm Title
septic shock TPT then TEE
Arm Type
Active Comparator
Arm Description
Group 1: Each patient will be assessed by both the transpulmonary thermodilution technique and transesophageal echocardiography (TEE)..
Arm Title
septic shock TEE then TPT
Arm Type
Active Comparator
Arm Description
Goup 2: Each patient will be assessed by both transesophageal echocardiography (TEE) and the transpulmonary thermodilution technique.
Intervention Type
Combination Product
Intervention Name(s)
early septic shock
Intervention Description
Each patient will be assessed by both the transpulmonary thermodilution and Transesophageal Echocardiography.
Primary Outcome Measure Information:
Title
therapeutic procedure following the hemodynamic assessment
Description
Changes in therapy proposed after the hemodynamic assessment (hemodynamic profile) by each of the two tested methods: blood volume expansion (preload responsiveness), positive inotrope (cardiac dysfunction), vasopressor (vasoplegia), no change in ongoing therapy or dose tapering (inotropes or vasopressor).
Time Frame
2 years
Secondary Outcome Measure Information:
Title
efficacy and safety of therapeutic intervention
Description
Efficacy (clinical problem solved) and tolerance (potential side-effects) of the therapeutic change.
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ventilated patient in sinus rhythm with septic shock requiring a hemodynamic assessment Exclusion Criteria: < 18 yr-old pregnancy contra-indication for TEE, non sinus rhythm, aplasia, prior participation to the study, hemodynamic assessment using any other technique than those tested in the study.
Facility Information:
Facility Name
Bordeaux UH
City
Bordeaux
ZIP/Postal Code
33 076
Country
France
Facility Name
Toulouse UH
City
Toulouse
ZIP/Postal Code
31 059
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
28866112
Citation
Vignon P, Begot E, Mari A, Silva S, Chimot L, Delour P, Vargas F, Filloux B, Vandroux D, Jabot J, Francois B, Pichon N, Clavel M, Levy B, Slama M, Riu-Poulenc B. Hemodynamic Assessment of Patients With Septic Shock Using Transpulmonary Thermodilution and Critical Care Echocardiography: A Comparative Study. Chest. 2018 Jan;153(1):55-64. doi: 10.1016/j.chest.2017.08.022. Epub 2017 Sep 1.
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Transpulmonary Thermodilution and Transesophageal Echocardiography in Early Septic Shock

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