Authorised Therapeutic use (Phase IV) Staphylococcus aureus bacteremia

Staphylococcus aureus Network Adaptive Platform trial (SNAP)

EU CTIS ID: 2023-503582-35-00

What this study is testing

To examine the effect on all-cause mortality at 90 days of a range of interventions in patients with SAB

  • Therapeutic use (Phase IV)

A plain-language read of the study's public EU CTIS listing. The study team confirms the details.

Who can take part

You may be able to join if

  • Staphylococcus aureus complex grown from ≥1 blood culture
  • Admitted to a participating hospital at the time of eligibility assessment (OR if patient has died, they were admitted to this site anytime from the time of blood culture collection until the time of eligibility assessment)

You likely can't join if

  • Time of anticipated platform entry is greater than 72 hours post collection of the index blood culture
  • Polymicrobial bacteraemia, defined as more than one organism (at species level) in the index blood cultures OR in any subsequent blood culture reported between the collection of the index blood culture and platform eligibility assessment, excluding those organisms judged to be contaminants by either the microbiology laboratory or treating clinician
  • Known previous participation in the randomised SNAP platform
  • Known positive blood culture for S. aureus (of the same silo: PSSA, MSSA or MRSA) between 72 hours and 180 days prior to the time of eligibility assessment
  • Treating team deems enrolment in the study is not in the best interest of the patient
  • Treating team believes that death is imminent and inevitable
See the full eligibility criteria
Who can join
  • Staphylococcus aureus complex grown from ≥1 blood culture
  • Admitted to a participating hospital at the time of eligibility assessment (OR if patient has died, they were admitted to this site anytime from the time of blood culture collection until the time of eligibility assessment)
What rules you out
  • Time of anticipated platform entry is greater than 72 hours post collection of the index blood culture
  • Polymicrobial bacteraemia, defined as more than one organism (at species level) in the index blood cultures OR in any subsequent blood culture reported between the collection of the index blood culture and platform eligibility assessment, excluding those organisms judged to be contaminants by either the microbiology laboratory or treating clinician
  • Known previous participation in the randomised SNAP platform
  • Known positive blood culture for S. aureus (of the same silo: PSSA, MSSA or MRSA) between 72 hours and 180 days prior to the time of eligibility assessment
  • Treating team deems enrolment in the study is not in the best interest of the patient
  • Treating team believes that death is imminent and inevitable
  • Patient is for end-of-life care and antibiotic treatment is considered not appropriate
  • Patient has died since the collection of the index blood culture

The study team makes the final eligibility decision.

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18-64 years, 65+ years. The study team makes the final eligibility decision.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from EU CTIS; the study team decides eligibility.