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NCT Number: NCT04291768

Shortened Antibiotic Treatment of 5 Days in Gram-negative Bacteremia

GNB5 is an investigator-initiated multicentre non-inferiority randomized controlled trial which aims to assess the efficacy and safety of shortened antibiotic for patients hospitalized with a Gram negative bacteremia with a urinary tract source of infection (GNB).

Five days after initiation of antimicrobial therapy for GNB, participants are randomized 1:1 to parallel treatment arms: 5 days (intervention) or minimum 7 days (control) of antibiotic treatment. The intervention group discontinues antibiotics at day 5 if clinically stable and afebrile. The control group receives antibiotics for a duration of 7 days or longer at the discretion of the treating physician.

The primary outcome is 90-day survival without clinical or microbiological failure to treatment, which will be tested with a non inferiority margin of 10%.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

University Hospital of Aalborg, Aalborg, Denmark

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About this study

Introduction: Prolonged use of antibiotics is closely related to antibiotic-associated infections, anti-microbial resistance and adverse drug events. The optimal duration of antibiotic treatment for Gram-negative bacteremia (GNB) with a urinary tract source of infection is poorly defined.

Methods and analysis: Investigator initiated multicenter, non-blinded, non-inferiority randomized controlled trial with two parallel treatment arms. One arm will receive shortened antibiotic treatment of 5 days and the other arm will receive standard antibiotic treatment of 7 days or longer. Randomization will occur in equal proportion (1:1) no later than day 5 of efficacious antibiotic treatment as determined by antibiogram. Immunosuppressed patients and those with GNB due to non-fermenting bacilli (Acinetobacter spp, Pseudomonas spp), Brucella spp, Fusobacterium spp or polymicrobial growth are ineligible.

Primary endpoint is 90-day survival without clinical or microbiological failure to treatment. Secondary endpoints include all-cause mortality, total duration of antibiotic treatment, hospital re-admission and Clostridioides difficile infection. Interim safety analysis will be performed after the recruitment of every 100 patients. Given an event rate of 12%, a margin of 10% and 90% power, the required sample size to determine non-inferiority is 380 patients. Analyses will be performed on both intention-to-treat and per-protocol populations.

Ethics and dissemination: Approval by Ethics Committee and National Competent Authorities will be obtained before initiation of the trial. Results of the main trial and each of the secondary endpoints will be submitted for publication in a peer-reviewed journal.

Impact: Demonstration of non-inferiority will provide needed evidence to safely shorten antibiotic treatment duration in GNB with a urinary tract source of infection and thereby reduce the risk of adverse events and development of resistance associated with use of antibiotics

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age >18 years
  • Blood culture positive for Gram-negative bacteria
  • Evidence of urinary tract source of infection (positive urine culture or at least one clinical symptom compatible with urinary tract infection)
  • Antibiotic treatment with antimicrobial activity to Gram-negative bacteria administrated within 12 hours of first blood culture
  • Temperature <37.8°C at randomization
  • Clinically stabile at randomization (systolic blood pressure > 90 mm Hg, heart rate <100 beats/min., respiratory rate <24/minute, peripheral oxygen saturation > 90 %)
  • Oral and written informed consent

Exclusion criteria

  • Antibiotic treatment (>2 day) with antimicrobial activity to Gram-negative bacteria within 14 days of inclusion
  • Gram-negative bacteremia within 30 days of blood culture
  • Immunosuppression (Untreated HIV-infection, Neutropenia (absolute neutrophil count < 1.0 x 109/l), Untreated terminal cancer, Receiving immunosuppressive agents (ATC-code L04A), Corticosteroid treatment (≥20 mg/day prednisone or the equivalent for >14 days) within the last 30 days, Chemotherapy within the last 30 days, Immunosuppressed after solid organ transplantation, Asplenia)
  • Polymicrobial growth in blood culture
  • Bacteremia with non-fermenting Gram-negative bacteria (Acinetobacter spp, Burkholderia spp, Pseudomonas spp), Brucella spp, or Fusobacterium spp
  • Failure to remove source of infection within 72 hours of first blood culture (e.g. change of catheter á demeure)
  • Pregnancy or breastfeeding

Treatment and study plan

Shortened antibiotic treatment

Other

Shortened antibiotic treatment of 5 days. Participation in the study will only affect treatment duration and will have no influence on the choice of treatment in respect to type and dose of antibiotic treatment.

Standard antibiotic treatment

Other

Standard antibiotic treatment of minimum 7 days at the discretion of treating physician. Participation in the study will only affect treatment duration and will have no influence on the choice of treatment in respect to type and dose of antibiotic treatment.

Primary outcomes

  1. 90-day survival without clinical or microbiological failure to treatment

    Time frame: 90 days

    90-day survival without clinical or microbiological failure to treatment as defined:

    • All-cause mortality from day of randomization and until day 90
    • Microbiological failure: Recurrent bacteremia due to the same microorganism as verified by sequence analysis occurring from day of randomization and until day 90
    • Clinical failure: Re-initiation of therapy against Gram-negative bacteremia for more than 48 hours due to clinical worsening suspected to be due to the initial infecting organism and for which there is no alternate diagnosis/pathogen suspected from the day of randomization and until day 90
    • Distant complications of initial infection, defined by growth of the same bacteria as in the initial bacteremia (e.g. endocarditis, meningitis)
    • Local suppurative complication that was not present at infection onset (e.g. renal abscess in pyelonephritis)

Secondary outcomes

  1. Mortality

    Time frame: 14, 30 and 90 days

    Number of deaths by any cause

  2. Total duration of antibiotic treatment

    Time frame: 90 days

    Days that the participant receives antibiotic treatment for Gram-negative bacteremia, adding intravenous and oral therapy

  3. Type of antibiotic treatment

    Time frame: 90 days

    Antibiotic treatment for Gram-negative bacteremia given by antibiogram

  4. Duration of antibiotic treatment

    Time frame: 90 days

    Duration of antibiotic treatment for Gram-negative bacteremia given by antibiogram

  5. Total length of hospital stay

    Time frame: 90 days

    Days from the date of hospital admission for Gram-negative bacteremia to the date of discharge

  6. Hospital re-admission

    Time frame: 30 and 90 days

    Number of participants with readmissions for reasons related to or unrelated to Gram-negative bacteremia

  7. Antibiotic adverse events

    Time frame: 90 days

    Number of participants with adverse events with possible relation to the antibiotic treatment of Gram-negative bacteremia

  8. Use of antimicrobials after discharge

    Time frame: 90 days

    Days of antibiotic treatment for any reason after hospital discharge

  9. Severe adverse events

    Time frame: 90 days

    Number of participants with serious adverse events according to International Council of Harmonisation-Good Clinical Practice (ICH-GCP) guidelines

  10. Acute kidney injury

    Time frame: 90 days

    Number of participants with acute kidney injury is defined according to RIFLE criteria as increased creatinine level x 1.5 from baseline or estimated glomerular filtration rate (eGFR) decrease >25% or urine output of <0.5 ml/kg/h for 6 hours.

  11. Clostridioides difficile infection

    Time frame: 90 days

    Number of participants with Clostridioides difficile infection

  12. Multidrug-resistance organism

    Time frame: 90 days

    Multidrug-resistance organism defined as identification of resistant bacteria in a clinical specimen obtained only from a clinical infection.

Study contacts

Contact information is provided by the study sponsor or research team.

Sandra Tingsgård, MD

CONTACT

[email protected]

+4520544094

Thomas Benfield, MD DMSc

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

Thomas Benfield

Other

Registry information

Official study title

Short Course Antibiotic Treatment of Gram-negative Bacteremia: A Multicenter, Randomized, Non-blinded, Non-inferiority Interventional Study

Acronym: GNB5

Important dates

Study start
2020
Primary completion
2026
Study completion
2026
First posted
Mar 2, 2020
Registry last updated
Feb 8, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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