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NCT Number: NCT06096025

Short Versus Long Duration of Therapy for Streptococcus Pneumoniae Bloodstream Infections

Streptococcus pneumoniae is a gram-positive (GP) bacteria responsible for common infections such as community-acquired pneumonia (CAP), as well as complicated infections such as bacteremia, infective endocarditis and meningitis. S. pneumoniae bacteremia ranks among the top 10 most common pathogens associated with bloodstream infections and correlates with high morbidity and mortality worldwide.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Methodist Dallas Medical Center

Dallas, Texas, 75203, United States

About this study

The Infectious Diseases Society of America (IDSA) guidelines for CAP management advocate for short courses of antibiotics for CAP treatment. However, it does not address duration of therapy for common CAP pathogens such as S. pneumoniae when associated with blood stream infections (BSI). 3

Currently, GP bacteremia duration of therapy typically ranges from 7 to 14 days based on IDSA guideline recommendations for Staphylococcus aureus bacteremia with no further definitive consensus.4 Additionally, lack of data and randomized clinical trials on the efficacy and safety of short compared to long treatment duration have led to variability in practice. Most randomized clinical trials as well as retrospective studies on treatment duration, have been conducted mainly in gram-negative BSI

Who can participate

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

Inclusion criteria

  • • ≥18 years of age
  • S. pneumoniae isolated from ≥1 blood cultures
  • Active IV antibiotic therapy within 48 hours of the first positive blood culture(7,8)
  • Clinical stability by day 10 of therapy

Exclusion criteria

  • • Treatment duration <5 days or >16 days
  • Death before completion of therapy (<10 days vs. ≥ 10 days )
  • Polymicrobial BSI
  • Invasive infection caused by S. pneumoniae (endocarditis, meningitis, and lung abscess)

Treatment and study plan

pneumoniae bacteremia therapy

Drug

To evaluate the effectiveness of short 10 days versus long (≥10 days) duration of therapy associated with S. pneumoniae bacteremia.

Other names: Total antibiotic treatment duration

Primary outcomes

  1. Infection related-hospitalization

    Time frame: 30 days

    hospital readmission with streptococcal pneumonia, bacteremia, endocarditis, meningitis, and lung abscess within 30 days of antibiotic completion

  2. Recurrence

    Time frame: 30 days

    Reinfection with streptococcal pneumonia, within 30 days of antibiotic completion

  3. All-cause mortality

    Time frame: 30 days

    Death within 30 days of antibiotic completion

Secondary outcomes

  1. ICU Length of stay(LOS)

    Time frame: 30 days

    length of ICU stay

  2. Hospital LOS

    Time frame: 30 days

    length of hospital stay

  3. Occurrence of C. difficile infection

    Time frame: 30 days

    Number of times of C.difficile infections

  4. Total antibiotic treatment duration

    Time frame: 30 days

    Number of times of antibiotic treatment duration

  5. Central venous catheter placement

    Time frame: 30 days

    placement of venous catheter

Sponsors and collaborators

Lead sponsor

Methodist Health System

Other

Registry information

Official study title

Short Versus Long Duration of Therapy for Streptococcus Pneumoniae Bloodstream

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Oct 23, 2023
Registry last updated
Jul 4, 2025

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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