Actively Recruiting
Provocation After Nurse-Directed Assessment (PANDA) Study
Led by The University of Hong Kong · Updated on 2026-04-29
440
Participants Needed
4
Research Sites
208 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The study aims to evaluate the effectiveness and safety of a collaborative nurse-allergist approach in penicillin allergy delabeling services. It also seeks to assess the impact on patients' quality of life and compare resource utilization and cost-effectiveness between the nurse-allergist collaborative approach and the traditional allergist-led approach.
CONDITIONS
Official Title
Provocation After Nurse-Directed Assessment (PANDA) Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Receiving inpatient or outpatient treatment at a participating hospital during the study period
- Having a documented penicillin allergy label
- Undergoing penicillin allergy evaluation by either the nurse-allergist collaborative approach or the traditional allergist-led approach
- Availability of required demographic and clinical data for the study
You will not qualify if you...
- Unable to provide a complete medication history or history of penicillin allergy
- Having only emergency or short-term treatment records
- Having taken steroids, antihistamines, or similar medications within the last 3 days
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 4 locations
1
Prince of Wales Hospital
Hong Kong, Hong Kong, 999077
Actively Recruiting
2
Princess Margaret Hospital
Hong Kong, Hong Kong, 999077
Actively Recruiting
3
Queen Elizabeth Hospital
Hong Kong, Hong Kong, 999077
Actively Recruiting
4
Queen Mary Hospital
Hong Kong, Hong Kong, 999077
Actively Recruiting
Research Team
E
Elaine Lee
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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