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Personalized Antibiotic Treatment in the Emergency Department: Panther Trial
This pilot study will randomize 40 female patients with acute uncomplicated pyelonephritis to receive standard duration of therapy versus patient-directed antimicrobial duration (PDAD). The primary objectives of this pilot trial are to determine the feasibility and safety of conducting a full-scale multi-center randomized controlled trial.
Following informed consent, patients will be randomized to receive 10 days of cephalexin or PDAD (minimum of 3 days of cephalexin followed by placebo once patient reports 24 hours of symptom resolution). Patients will be evaluated at day 1 in-person, then daily using a mobile cellphone application to assess acute uncomplicated pyelonephritis (AUP) symptoms and quality of life (QOL). Urine samples will be collected at in-person visits at day 1, 3 weeks, and 4 weeks. Study feasibility will be assessed through day 90.
Age
18 - 55 years
Sex
FEMALE
Healthy Volunteers
Yes
Olive View - UCLA Medical Center
Sylmar, California, United States
University of Iowa Hospitals and Clinics
Iowa City, Iowa, United States
Start Date
June 4, 2024
Primary Completion Date
August 29, 2025
Completion Date
August 29, 2025
Last Updated
September 12, 2025
35
ACTUAL participants
Cephalexin
DRUG
Cephalexin or placebo
DRUG
Lead Sponsor
Brett A Faine
Collaborators
Data Source & Attribution
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