Staphylococcus Aureus Network Adaptive Platform Trial

NCT05137119 · Status: RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 8000

Last updated 2026-05-06

No results posted yet for this study

Summary

The Staphylococcus aureus Network Adaptive Platform (SNAP) trial is an International Multi-Centered Randomised Adaptive Platform Clinical Trial to evaluate a range of interventions to reduce mortality for patients with Staphylococcus Aureus bacteraemia (SAB).

Conditions

  • Staphylococcus Aureus Bacteremia

Interventions

DRUG

Cefazolin

Cefazolin

DRUG

Penicillin

benzylpenicillin

DRUG

Clindamycin

Clindamycin

DRUG

Vancomycin

Vancomycin or Daptomycin

OTHER

Effectiveness of early switch to oral antibiotics

This involves testing a strategy rather than individual antibiotic agents

RADIATION

Whole body FDG PET/CT Imaging

Whole body FDG PET/CT imaging will be performed using a standardised protocol describing patient preparation and minimum specifications for radiopharmaceutical production, quality control, and PET/CT acquisition.

Sponsors & Collaborators

  • Berry Consultants

    collaborator OTHER
  • McGill University Health Centre/Research Institute of the McGill University Health Centre

    collaborator OTHER
  • Menzies School of Health Research

    collaborator OTHER
  • Aotearoa Clinical Trials

    collaborator OTHER
  • Queensland University of Technology

    collaborator OTHER
  • Sunnybrook Health Sciences Centre

    collaborator OTHER
  • Tan Tock Seng Hospital

    collaborator OTHER
  • Telethon Kids Institute

    collaborator OTHER
  • The Peter Doherty Institute for Infection and Immunity

    collaborator OTHER
  • The University of Queensland

    collaborator OTHER
  • UMC Utrecht

    collaborator OTHER
  • Radboud University Medical Center

    collaborator OTHER
  • King's College London

    collaborator OTHER
  • Rambam Health Care Campus

    collaborator OTHER
  • University College, London

    collaborator OTHER
  • The Methodist Hospital Research Institute

    collaborator OTHER
  • University of Melbourne

    lead OTHER

Principal Investigators

  • Prof Steven Tong · University of Melbourne / Melbourne Health

  • Prof Joshua Davies · Menzies School of Research / Hunter New England Medical Centre

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
FACTORIAL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-02-16
Primary Completion
2028-12-01
Completion
2028-12-01

Countries

  • United States
  • Australia
  • Canada
  • France
  • Germany
  • Israel
  • Japan
  • Netherlands
  • New Zealand
  • Singapore
  • South Africa
  • Sweden
  • United Kingdom

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05137119 on ClinicalTrials.gov