A Pilot Proof of Concept Single-Center Study of the Use of Oritavancin in Systemic Staphylococcus aureus Infections in Patients with Opioid Use Disorder

  • STATUS
    Recruiting
  • participants needed
    15
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Updated on 19 February 2024

Summary

The study participants will be in the study for approximately 2 months including the screening, intervention phase and the 6 weeks of follow-up time

Details
Condition Staphylococcus Aureus Bacteremia | Staphylococcus Aureus Endocarditis
Age 99years or below
Clinical Study IdentifierTBD
Last Modified on19 February 2024

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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