ClinConnect ClinConnect Logo
Search / Trial NCT06637332

Daptomycin Vs. Vancomycin for the Treatment of Methicillin Resistant S. Aureus Bacteremia

Launched by TODD C. LEE MD MPH FIDSA · Oct 9, 2024

Trial Information

Current as of July 01, 2025

Recruiting

Keywords

S. Aureus Bacteremia Methicllin Resistant Mrsa S. Aureus Bloodstream Infection Daptomycin Vancomycin

ClinConnect Summary

This clinical trial is studying how effective two common antibiotics, vancomycin and daptomycin, are in treating serious bloodstream infections caused by a type of bacteria called methicillin-resistant Staphylococcus aureus (MRSA). The goal is to see which of these medications works better for patients who have this difficult-to-treat infection. The trial is currently looking for participants aged 65 and older who have a confirmed MRSA bloodstream infection. However, individuals who have severe allergies to either of the medications or certain complications, like MRSA pneumonia, may not be eligible to join.

If you or a family member decides to participate in this trial, you will receive one of the two antibiotics as part of your treatment. The trial is open-label, meaning both you and the researchers will know which antibiotic you are receiving. Participants will have regular check-ups to monitor their health and response to the treatment. This study is part of a larger research effort to improve how we treat MRSA infections, and your involvement could help advance medical knowledge and potentially benefit others facing similar health challenges.

Gender

ALL

Eligibility criteria

  • The participant must meet all inclusion and exclusion criteria for the SNAP Platform (NCT05137119) and also the following inclusion and exclusion criteria:
  • Inclusion Criteria:
  • Methicillin-resistant S. aureus bacteremia
  • Exclusion Criteria:
  • Severe allergy or non-severe rash to vancomycin or daptomycin
  • Suspected or confirmed MRSA pneumonia
  • Known vancomycin minimum inhibitory concentration (MIC) greater than or equal to 2mg/L or daptomycin MIC greater than or equal to 1mg/L

About Todd C. Lee Md Mph Fidsa

Dr. Todd C. Lee, MD, MPH, FIDSA, is a distinguished clinical trial sponsor with extensive expertise in infectious diseases and public health. With a robust academic background and a commitment to advancing medical research, Dr. Lee leads innovative clinical trials focused on improving patient outcomes and developing novel therapeutic interventions. His multidisciplinary approach combines clinical excellence with strategic insights into epidemiology and healthcare practices, fostering collaborations that drive impactful research initiatives. Dr. Lee's dedication to advancing scientific knowledge and enhancing patient care positions him as a key contributor in the field of clinical trials.

Locations

Montreal, Quebec, Canada

Surrey, British Columbia, Canada

Patients applied

0 patients applied

Trial Officials

Todd C Lee, MD MPH FIDSA

Principal Investigator

McGill University Health Centre/Research Institute of the McGill University Health Centre

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported