Published December 2, 2022 | Version 3.00
Journal article Open

Protocolised REDUction of non-resuscitation fluids versus usual care in SEptic shock patients (REDUSE) - a statistical analysis plan for a multicentre feasibility trial

Authors/Creators

  • 1. Copenhagen Trial Unit, Centre for Clinical Intervention Research, Copenhagen University Hospital − Rigshospitalet, Copenhagen, Denmark.
  • 2. Anaesthesia and Intensive Care, Department of Clinical sciences Lund, Lund University, Helsingborg Hospital, Helsingborg, Sweden
  • 3. Neurology, Department of Clinical Sciences Lund, Lund University, Skane University Hospital, Lund, Sweden,
  • 4. Intensive and perioperative care, Skane university hospital, Malmö, Sweden. Department of clinical sciences Lund university, Lund, Sweden.
  • 5. Department of Operation and Intensive Care, Hallands Hospital Halmstad, Halmstad, Sweden
  • 6. Anaesthesia and Intensive Care, Department of Clinical sciences Lund, Lund University, Skåne University Hospital, Lund, Sweden
  • 7. Anaesthesia and Intensive Care, Department of Clinical sciences Lund, Lund University, Kristianstad Hospital, Kristianstad, Sweden
  • 8. Anaesthesia and Intensive Care, Östersund Hospital. Department of Surgery and Perioperative Sciences, Umeå University, Umeå, Sweden
  • 9. Department of Anaesthesiology and Intensive Care Medicine, Institute of Clinical Sciences, University of Gothenburg, Gothenburg, Sweden
  • 10. Department of Surgical Sciences, Anaesthesiology and Intensive Care, Uppsala University, Sweden, Department of Surgical Sciences, Hedenstierna laboratory, Uppsala University, Sweden

Description

Protocolised REDUction of non-resuscitation fluids versus usual care in SEptic shock patients (REDUSE) - a statistical analysis plan for a multicentre feasibility trial

The objective of this trial is to assess the feasibility of a trial comparing a protocolised reduction in administration of non-resuscitation fluids to usual care in patients with septic shock. Here, we describe the statistical analysis plan for this feasibility trial.

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