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NCT05453565 | NOT YET RECRUITING | Septic Shock


Restricted or Liberal Fluid for Haemodynamic Resuscitation in Sepsis
Sponsor:

Australian and New Zealand Intensive Care Research Centre

Brief Summary:

A prospective, individual patient data meta-analysis (IPDMA) of four multicentre, open-label, randomised clinical trials of initial haemodynamic resuscitation in patients with septic shock.

Condition or disease

Septic Shock

Fluid Resuscitation

Intervention/treatment

Vasopressors

Fluids

Detailed Description:

This study is a prospective, individual patient data meta-analysis (IPDMA) of four multicentre, open-label, randomised clinical trials of initial haemodynamic resuscitation in patients with septic shock. The investigators will include four multicentre, open-label, randomised, clinical trials: * Australasian Resuscitation in Sepsis Evaluation Fluids of Vasopressors in Emergency Department Sepsis (ARISE FLUIDS) trial conducted in Australia and New Zealand. ClinicalTrials.gov identifier NCT04569942 * Conservative versus Liberal Approach to fluid therapy of Septic Shock in intensive Care (CLASSIC) trial conducted in seven European countries. ClinicalTrials.gov identifier NCT03668236 * Crystalloid Liberal or Vasopressors Early (CLOVERS) trial conducted in the United States. ClinicalTrials.gov identifier NCT03434028 * Early Vasopressors in Sepsis (EVIS) trial conducted in the United Kingdom. ClinicalTrials.gov identifier NCT05179499 All four trials have all received relevant approval from a research ethics committee with a locally appropriate method of obtaining consent. These trials are prospectively chosen prior to the results of any individual trial being known because they are investigating the same broad question in patients with acute septic shock across several countries. The investigators of these trials collaborated to harmonise data and outcomes as far as possible across all trials to facilitate an IPDMA. The aims to provide high level evidence to address the question of whether a fluid sparing/early vasopressor approach or a liberal fluid/later vasopressor approach to initial haemodynamic resuscitation in septic shock results in improved outcomes, including mortality.

Study Type : OBSERVATIONAL
Estimated Enrollment : 7838 participants
Official Title : Fluid Restricted Resuscitation in Sepsis With Hypotension Meta-Analysis (FRESHLY): Individual Patient Data Met-analysis of the ARISE FLUIDS, CLASSIC, CLOVERS and EVIS Trials
Actual Study Start Date : 2025-11
Estimated Primary Completion Date : 2026-11
Estimated Study Completion Date : 2026-11

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • Participants of the ARISE FLUIDS, CLASSIC, CLOVERS \& EVIS trials who had
    • * Suspected or proven infection
    • * Systolic blood pressure (SBP) \<100 mm Hg OR mean arterial pressure (MAP) \<65 mm Hg
    • * Lactate ≥ 2.0 mmol/L
    • * Requirement for vasopressors to meet perfusion targets
    • Exclusion criteria
      • Participants not in the ARISE FLUIDS, CLASSIC, CLOVERS \& EVIS trials

Restricted or Liberal Fluid for Haemodynamic Resuscitation in Sepsis

Location Details

NCT05453565


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