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Seven Versus Fourteen Days of Treatment in Uncomplicated Staphylococcus Aureus Bacteremia (SAB7)

Primary Purpose

Staphylococcus Aureus Bacteremia

Status
Unknown status
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Antibiotic therapy duration for 7 days
Sponsored by
Thomas Benfield
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Staphylococcus Aureus Bacteremia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age > 18 years
  • Blood culture positive for Staphylococcus aureus
  • Antibiotic treatment with antimicrobial activity to S. aureus administrated within 12 hours of the first positive blood culture
  • Temperature < 37,5 degrees celsius at randomization
  • S. aureus negative follow-up blood culture obtained 48-96 hours after microbiological verified SAB.
  • Patients written consent obtained

Exclusion Criteria:

  • Persistence of S. aureus bacteremia before randomization (S. aureus positive follow-up blood culture obtained 48-96 hours of the first positive blood culture)
  • Polymicrobial infection
  • Antibiotic treatment whit no antimicrobial activity to S. aureus administrated more than 12 hours of the first positive blood culture
  • Endocarditis or other intracardiac infection demonstrated with transthoracic or transesophageal echocardiography
  • Previous history of endocarditis
  • Pacemaker or other intracardiac implant
  • Failure to remove a likely focus of infection, such as central venous catheter within 72 hours of the first positive blood culture.
  • Prosthetics in joints and bones or vascular grafts
  • Pneumonia or infection involving bone or joints
  • Previously bone/join infection
  • S. aureus infection within the last 90 days
  • Pregnancy or breastfeeding
  • Neutropenia (blood neutrophils < 1,0 x 109/l)
  • Untreated cancer
  • Chemotherapy within 90 days.

Sites / Locations

  • Hvidovre HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Antibiotic therapy duration for 7 days

Antibiotic therapy duration for 14 days

Arm Description

Outcomes

Primary Outcome Measures

90-day survival without clinical or microbiological failure to treatment or relapse

Secondary Outcome Measures

Microbiologically failure to treatment
Verified S. aureus infection of the same genotype as the initial infection
Microbiologically relapse
Verified S. aureus infection of the same genotype as the initial infection
Clinical failure to treatment or relapse
Initiation of anti-staphylococcal therapy for more than 48 hours due to suspected recurrence.
Mortality
All-cause mortality
Severe adverse events
grade 3 or above adverse events
Acute renal injury
A 1.5 fold increase in creatinine or a 25% decrease of the glomerular filtration rate (GFR)
Clostridium difficile infection
Microbiologically verified C. difficile infection
Multidrug-resistance organism
Microbiologically verified multidrug-resistance organism
Health-associated costs
Public health related cost estimated from a general consideration of the expenses associated with hospitalization for SAB.

Full Information

First Posted
November 10, 2017
Last Updated
October 14, 2020
Sponsor
Thomas Benfield
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1. Study Identification

Unique Protocol Identification Number
NCT03514446
Brief Title
Seven Versus Fourteen Days of Treatment in Uncomplicated Staphylococcus Aureus Bacteremia
Acronym
SAB7
Official Title
Efficacy of Seven and Fourteen Days of Antibiotic Treatment in Uncomplicated Staphylococcus Aureus Bacteremia: A Randomized, Non-blinded, Non-inferiority Interventional Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Unknown status
Study Start Date
June 1, 2018 (Actual)
Primary Completion Date
May 1, 2021 (Anticipated)
Study Completion Date
November 1, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Thomas Benfield

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
Introduction: Staphylococcus aureus bacteremia (SAB) plays an important role in long-course antibiotic therapy. Current international guidelines recommend fourteen days of intravenous antibiotic treatment for SAB in order to minimize risks of secondary deep infections and complications. However, patients with simple SAB are known to have a low risk of complications. Reducing treatment length in uncomplicated SAB would reduce the total consumption of antibiotics, adverse events and duration of hospital admission. SAB7 seeks to determine if seven days of antibiotic treatment in patients with uncomplicated SAB is non-inferior to fourteen days of treatment. Method: The study is designed as a randomized, non-blinded, non-inferiority interventional study. Primary measure of outcome will be failure to treatment or recurrence of SAB twelve weeks after termination of antibiotic treatment. As a measure of secondary outcome the prevalence of severe adverse effects will be evaluated, in particular secondary infection with Clostridium difficile, mortality as well as public health related costs. Patients identified with uncomplicated SAB, are randomized 1:1 in two parallel arms to seven or fourteen days of antimicrobial treatment, respectively. Endpoints will be tested with a statistical non-inferiority margin of 10%. Conclusion: SAB 7 will determine if seven days of antibiotic treatment in patients with uncomplicated SAB is sufficient and safe, potentially modifying current treatment recommendations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Staphylococcus Aureus Bacteremia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
284 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Antibiotic therapy duration for 7 days
Arm Type
Experimental
Arm Title
Antibiotic therapy duration for 14 days
Arm Type
No Intervention
Intervention Type
Drug
Intervention Name(s)
Antibiotic therapy duration for 7 days
Intervention Description
Antibiotic therapy for seven days
Primary Outcome Measure Information:
Title
90-day survival without clinical or microbiological failure to treatment or relapse
Time Frame
up to 90 days
Secondary Outcome Measure Information:
Title
Microbiologically failure to treatment
Description
Verified S. aureus infection of the same genotype as the initial infection
Time Frame
less than 7 days after treatment termination
Title
Microbiologically relapse
Description
Verified S. aureus infection of the same genotype as the initial infection
Time Frame
more than 7 days after treatment termination
Title
Clinical failure to treatment or relapse
Description
Initiation of anti-staphylococcal therapy for more than 48 hours due to suspected recurrence.
Time Frame
Up to day 90
Title
Mortality
Description
All-cause mortality
Time Frame
Days 14, 28, 90 and 180
Title
Severe adverse events
Description
grade 3 or above adverse events
Time Frame
Up to 26 weeks
Title
Acute renal injury
Description
A 1.5 fold increase in creatinine or a 25% decrease of the glomerular filtration rate (GFR)
Time Frame
Up to 26 weeks
Title
Clostridium difficile infection
Description
Microbiologically verified C. difficile infection
Time Frame
Up to 26 weeks
Title
Multidrug-resistance organism
Description
Microbiologically verified multidrug-resistance organism
Time Frame
Up to 26 weeks
Title
Health-associated costs
Description
Public health related cost estimated from a general consideration of the expenses associated with hospitalization for SAB.
Time Frame
Up to 26 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 years Blood culture positive for Staphylococcus aureus Antibiotic treatment with antimicrobial activity to S. aureus administrated within 12 hours of the first positive blood culture Temperature < 37,5 degrees celsius at randomization S. aureus negative follow-up blood culture obtained 48-96 hours after microbiological verified SAB. Patients written consent obtained Exclusion Criteria: Persistence of S. aureus bacteremia before randomization (S. aureus positive follow-up blood culture obtained 48-96 hours of the first positive blood culture) Polymicrobial infection Antibiotic treatment whit no antimicrobial activity to S. aureus administrated more than 12 hours of the first positive blood culture Endocarditis or other intracardiac infection demonstrated with transthoracic or transesophageal echocardiography Previous history of endocarditis Pacemaker or other intracardiac implant Failure to remove a likely focus of infection, such as central venous catheter within 72 hours of the first positive blood culture. Prosthetics in joints and bones or vascular grafts Pneumonia or infection involving bone or joints Previously bone/join infection S. aureus infection within the last 90 days Pregnancy or breastfeeding Neutropenia (blood neutrophils < 1,0 x 109/l) Untreated cancer Chemotherapy within 90 days.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Louise Thorlacius-Ussing, MD
Phone
+45 26457710
Email
louise.thorlacius-ussing@regionh.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Thomas Benfield, MD, DMSc
Email
Thomas.Lars.Benfield@regionh.dk
Facility Information:
Facility Name
Hvidovre Hospital
City
Hvidovre
State/Province
Copenhagen
ZIP/Postal Code
2650
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Louise Ussing, MD
Phone
26457710
Email
louise.thorlacius-ussing@regionh.dk

12. IPD Sharing Statement

Plan to Share IPD
No
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26061852
Citation
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Links:
URL
https://ctep.cancer.gov/protocoldevelopment/electronic_applications/ctc.htm
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