Epidemiology of Antimicrobial-use and Antimicrobial-resistant Infections in Four Hospitals in Thailand

NCT07082465 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 108000

Last updated 2025-07-24

No results posted yet for this study

Summary

The main goal of this retrospective observational study is to understand how stepping down antibiotic treatment (called antibiotic de-escalation) affects patients who receive it compared to those who don't after received a short-course (≤7 days) of parenteral antibiotics. The investigators will use past medical records from four public referral hospitals in Thailand from the year 2019 to 2024. The investigators will firstly evaluate which types of patients are more likely to receive antibiotic de-escalation. Then, the investigators will estimate the impact of antibiotic de-escalation, while taking those differences into account. This way, it will help us understand the impact of antibiotic de-escalation in real-world clinical practice. The investigators also aim to assess how accurate automated outbreak detection systems are at detecting outbreaks, evaluate patterns of antimicrobial use and antimicrobial-resistant infections, and develop new indicators for antimicrobial stewardship that are applicable for local and national actions in low and middle-income countries.

Conditions

  • Drug Resistance
  • Bacterial
  • Bacteremia

Sponsors & Collaborators

  • Wellcome Trust

    collaborator OTHER
  • University of Oxford

    lead OTHER

Principal Investigators

  • Direk Limmathurotsakul, MD, PhD · Mahidol Oxford Tropical Medicine Research Unit

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-08-01
Primary Completion
2026-08-16
Completion
2026-08-16

Countries

  • Thailand

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07082465 on ClinicalTrials.gov