Geisinger Antibiotic Allergy Pilot Program: Assess and Address
Stopped early · Early Phase 1
Conditions studied: Penicillin Allergy
In brief
This is a prospective non-inferiority study to evaluate penicillin allergy history in patients with reported penicillin allergy, who require penicillin or penicillin-derivative antibiotic during inpatient admission using a focused questionnaire. A simplified scoring system will be assigned to patient responses, and the total score will be utilized to identify low-risk patients that have a minimal risk of allergic reactions on exposure to penicillin or its derivative. Patients determined to have low risk based on this questionnaire will be offered a test dose (graded challenge) of amoxicillin in a supervised setting, and if they tolerate it, penicillin allergy label will be removed from patient's chart. We hypothesize that at least 95% of low-risk patients will successfully pass the graded amoxicillin challenge so the penicillin allergy label can be removed from their charts. A proportion as low as 0.85 would be a good clinical outcome and considered non-inferior to the expected proportion of 0.95.
Key facts
- Study ID
- NCT05464615
- Run by
- Geisinger Clinic
- People needed
- 20
- Starts
- 2024-03-04
- Expected to finish
- 2026-01-20
- Last updated by the study team
- 2026-07-20
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Hospitalized male or female patients with a history of Penicillin (PCN) allergy or PCN-derivative allergy as reported by patient or documented in Epic
- ≥18 years of age
- Patients with a medical need for treatment with a PCN or PCN-derivative or other beta-lactam antibiotics as determined by an inpatient provider
- Able and willing to provide consent in English.
You may not qualify if…
- History of documented immediate-onset severe allergic reaction or delayed onset hypersensitivity reaction to a PCN or PCN-derivative
- Patients who are hemodynamically unstable (e.g., pulse oximetry O2 saturation <90 %, respiratory rate >=21 per minute, severe hypoxia requiring non-invasive ventilation, high-flow nasal canula, or mechanical ventilation, refractory hypotension requiring vasopressor support, heart rate >100 beats per minute, etc.)
- Patients with uncontrolled pulmonary diseases (like exacerbation of asthma, Chronic Obstructive Pulmonary Disease (COPD), and/or other forms of chronic lung diseases)
Where it is running
- Geisinger Medical Center — Danville, Pennsylvania, United States
- Geisinger Lewistown Hospital — Lewiston, Pennsylvania, United States
- Geisinger Community Medical Center — Scranton, Pennsylvania, United States
- Geisinger Wyoming Valley — Wilkes-Barre, Pennsylvania, United States
Full record on ClinicalTrials.gov
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