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Targeted Tissue Perfusion Versus Macrocirculatory-guided Standard Care in Patients With Septic Shock (TARTARE-2S)

H

Helsinki University Central Hospital (HUCH)

Status

Completed

Conditions

Shock; Septic
Critical Illness

Treatments

Other: Hemodynamical treatment MCG
Other: Hemodynamical treatment TTP

Study type

Interventional

Funder types

Other

Identifiers

NCT02579525
TARTARE-2S-01

Details and patient eligibility

About

Background: The recommended monitoring and target levels in septic shock (SSC Guidelines 2012) including mean arterial pressure (MAP) target are not based on robust clinical data.

Objective: To test, if in patients with septic shock, tissue perfusion guided (TPG) treatment strategy leads to a faster resolution of hypoperfusion than the macrocirculatory target guided standard care.

Design: A prospective phase II two-parallel-group open-label randomized controlled trial

Interventions:

  1. Intervention group- Targeted tissue perfusion guided (TTP) - care.
  2. Control group - Macrocirculatory - guided (MCG) care.

Randomization: 1:1 stratified according to the site and presence or absence of known hypertension.

Trial size: 200 randomised patients in 4 ICUs.

Full description

Study hypothesis: Targeting at clinical tissue perfusion (in the TTP arm) will decrease the use and untoward effects of vasopressors, and result in more days alive in 30-days without vasopressor or inotropic support and without lactatemia, in comparison with standard clinical care with preference of macrocirculatory targets (MCG arm).

Intervention group - Targeted tissue perfusion (TTP) care:

Primary targets /registration period

  1. capillary refill time (CRT) / <3 sec/ every hour

  2. skin mottling / absent / every hour

  3. arterial lactate / <2.0 mmol/l/ per 2hr

  4. peripheral temperature/ warm /every hour

  5. urine output/ ≥0.5 mL/kg per hour/ every hour

  6. mean arterial pressure (MAP) 50-65 mmHg (minimum as a safety limit)/ continuous

    • if previous hypertension 65- 70 mmHg
    • if oliguria 2-hour trial 75-80 mmHg (If diuresis better, continue 2hr and re-evaluate) Secondary target
  7. Continuous mixed venous saturation (SvO2) >65%, if available

Control group - Macrocirculatory targets guided (MCG) standard care Primary targets

  1. Mean arterial pressure (MAP) 65-75 mmHg /continuous

    ** if previous hypertension 75-80 mmHg

    *** if oliguria < 0.3 ml/kg, 2-hour trial 85-90 mmHg (If diuresis better, continue 2hr and re-evaluate)

  2. Central venous pressure (CVP)/hourly, Adequate fluid therapy is indicated to restore clinical hypovolemia up to the recommended CVP-level of 8-12 mmHg, if needed

  3. Urine output ≥ 0.5 mL/kg/h/ hourly Secondary target

  4. Continuous SvO2 >65%, if available

Enrollment

200 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Septic shock defined as

    1. Septic infection AND
    2. systemic mean blood pressure > 65 mmHg requiring any dose of vasopressors (norepinephrine, vasopressin) despite adequate fluid resuscitation (minimum of 20 ml/kg crystalloids) AND
    3. Elevated lactate ≥ 3.0 mmol/L with suspected hypoperfusion

Exclusion criteria

  • aged less than 18 or over 80 years
  • any other probable condition than sepsis affecting or expected to affect the central nervous system including post cardiac arrest
  • present or suspected myocardial ischemia
  • acute pulmonary embolism
  • terminal illness and not considered for full intensive care support
  • use of extra-corporeal membrane oxygenation (ECMO)
  • known liver disease - Child-Pugh -Class B or C
  • confirmed chronic kidney disease known on admission
  • known to be pregnant or lactating
  • more than 4 hours from fulfilled inclusion criteria to randomization
  • another probable cause of hyperlactatemia
  • patients transferred from another ICU
  • patients with active haematological malignancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

200 participants in 2 patient groups

Targeted tissue perfusion guidance (TTP)
Experimental group
Description:
TTP-guidance based on clinical signs of peripheral perfusion.
Treatment:
Other: Hemodynamical treatment TTP
Macrocirculatory - guidance (MCG)
Active Comparator group
Description:
MCG-guidance based on recommended macrocirculatory parameters.
Treatment:
Other: Hemodynamical treatment MCG

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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