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Clinical Outcomes in Candidemia Patients Based on in Vitro Susceptibility

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University of Houston

Status

Completed

Conditions

Candida
Blood Stream Infections

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT01077336
G098881

Details and patient eligibility

About

Susceptibility testing is commonly employed in patients with bacterial infections in order to guide rational use of antibiotics; however, the use of antifungal susceptibility testing is limited due to lack of availability, costs, and delays in receiving results. The goals of antifungal susceptibility testing should mirror those of antibacterial susceptibility testing: to predict clinical response or failure. Additionally, susceptibility reports should be used as a guide for physicians when transitioning patients from parenteral to oral antifungal agents. Currently, it is unknown whether antifungal susceptibility testing impacts treatment decisions in hospitals that routinely perform Candida susceptibility testing. The purpose of this study is to evaluate the changes in antifungal treatment based on in vitro susceptibility reports and how these decisions affect mortality, recurrence of infection, and length of hospital stay in candidemia patients.

Enrollment

450 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hospitalized patients with bloodstream infections due to Candida species

Exclusion criteria

  • Patients will be excluded from this study if their medical charts contain incomplete outcome or susceptibility data. Patients treated empirically or definitively with amphotericin-based products will also be excluded

Trial design

450 participants in 1 patient group

Hospitalized patients with candidemia

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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