A Study Comparing Short-course Antifungal Therapy (SCAT) 7 Day vs Standard 14 Day Antifungal Therapy for Uncomplicated Candidemia
Launched by AUGUSTA UNIVERSITY · Apr 1, 2025
Trial Information
Current as of July 23, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is investigating whether a shorter, seven-day treatment with antifungal medication is as effective as the standard 14-day treatment for patients with uncomplicated candidemia, which is a type of infection caused by yeast in the bloodstream. The goal is to see if the shorter treatment can help patients recover just as well without causing more side effects or increasing the risk of death.
To participate in this trial, you need to be at least 18 years old and have a confirmed case of uncomplicated candidemia, meaning there are no signs of a more serious infection. You should not have received more than five days of antifungal treatment before joining the study. If you decide to participate, you will be randomly assigned to receive either the seven-day or the 14-day treatment. The trial is not currently recruiting participants, so it’s important to keep an eye out for updates if you or someone you know might be interested in joining.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Patients ≥ 18 years of age
- • 2. Uncomplicated candidemia (positive blood culture only). No evidence of invasive candidiasis at day 1 or until day 7.
- • 3. Received \< 5 days of prior antifungal therapy
- • 4. Informed Consent for randomization
- • 5. Patients that did not consent to randomization have consented to be used as a natural history (controls) and will allow collection of available data from the medical record.
- Exclusion Criteria:
- • 1. Inadequate source control (e.g., unable to remove endovascular devices, urinary catheters).
- • 2. Invasive candidiasis of any type (e.g., deep seated candidiasis from sources other than blood)
- • 3. Abnormal LFTs \> 10-fold
- • 4. Greater than 5 days of prior antifungal therapy
- • 5. Endovascular devices that cannot be removed.
- • 6. Immunocompromised patients (AIDS/HIV; solid organ transplant, bone marrow transplant patients, oncology patients receiving chemotherapy, neutropenic patients (ANC of \< 1,500 cells/L
- • 7. Neutropenic at time of consent (what does this mean)
- • 8. Break-through candidemia (people with prior candidemia who relapsed) after treatment with antifungal therapy)
- • 9. Unable to provide informed consent from either the patient or legally authorized authority (LAR)
- • 10. Expected mortality within 96 hours
About Augusta University
Augusta University is a prominent academic institution dedicated to advancing healthcare through innovative research and clinical trials. As a leader in medical education and patient care, Augusta University conducts rigorous clinical studies aimed at improving treatment outcomes and enhancing patient quality of life. The university’s commitment to interdisciplinary collaboration fosters a dynamic research environment, enabling the exploration of novel therapies and interventions across a wide range of medical fields. With a focus on ethical standards and patient safety, Augusta University strives to translate scientific discoveries into tangible benefits for the community and beyond.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Augusta, Georgia, United States
Patients applied
Trial Officials
Jose Vazquez, MD
Principal Investigator
Augusta University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported