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

Who is this study for? Adult patients with Gram-Negative Bacteremia
What treatments are being studied? Antibiotics
Status: Recruiting
Location: See all (13) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

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%.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Denmark
University Hospital of Aalborg
NOT_YET_RECRUITING
Aalborg
University Hospital of Aarhus
NOT_YET_RECRUITING
Aarhus
Bispebjerg Hospital
RECRUITING
Copenhagen
Rigshospitalet
NOT_YET_RECRUITING
Copenhagen
Gentofte Hospital
RECRUITING
Hellerup
Herlev Hospital
RECRUITING
Herlev
Herning Hospital
NOT_YET_RECRUITING
Herning
Nordsjaellands Hospital
RECRUITING
Hillerød
Hvidovre Hospital
RECRUITING
Hvidovre
Kolding Hospital
NOT_YET_RECRUITING
Kolding
Odense University Hospital
NOT_YET_RECRUITING
Odense
Roskilde Hospital
NOT_YET_RECRUITING
Roskilde
Regionshospitalet Silkeborg
NOT_YET_RECRUITING
Silkeborg
Contact Information
Primary
Sandra Tingsgård, MD
sandra.tingsgaard@regionh.dk
+4520544094
Backup
Thomas Benfield, MD DMSc
thomas.lars.benfield@regionh.dk
Time Frame
Start Date: 2020-03-11
Estimated Completion Date: 2026-10-01
Participants
Target number of participants: 380
Treatments
Experimental: Intervention group
Shortened antibiotic treatment of 5 days
Active_comparator: Control group
Standard antibiotic treatment of minimum 7 days at the discretion of treating physician
Authors
Sandra Hansen
Related Therapeutic Areas
Sponsors
Leads: Thomas Benfield

This content was sourced from clinicaltrials.gov