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临床试验/NCT07127835
NCT07127835尚未招募不适用

Provocation After Nurse-Directed Assessment (PANDA) Study

The University of Hong Kong4 个研究点 分布在 1 个国家目标入组 440 人开始时间: 2025年9月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
440
试验地点
4
主要终点
Delabelling Success Rate

研究概览

简要总结

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.

详细描述

This study hypothesizes that by involving both nurses and allergists in the delabeling process and categorizing patients based on risk levels, it will achieve comparable success rates, safety, and improvements in patients' quality of life. This approach is expected to offer superior advantages in terms of time efficiency, resource utilization, and cost-effectiveness compared to traditional allergist-led services.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Receiving inpatient or outpatient treatment at a participating hospital during the study period;
  • Possessing a documented penicillin allergy label;
  • Underwent penicillin allergy evaluation by the nurse-allergist collaborative approach or the traditional allergist-led approach
  • Demographic and clinical data required for the study available.

排除标准

  • Patients unable to provide a complete medication history or history of penicillin allergy;
  • Patients with only emergency or short-term treatment records;
  • Patients who have taken steroids, antihistamines, or similar medications within the last 3 days.

结局指标

主要结局

Delabelling Success Rate

时间窗: 6 months

Assess the proportion of low-risk patients who are no longer considered allergic to penicillin after delabeling.

次要结局

  • Health-Related Quality of Life(6 months)
  • Antibiotic Usage Rate(6 months)
  • Age Group Analysis(6 months)
  • Immunocompetence Status(6 months)
  • Initial vs. Recurrent Labeling(6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Prof. Sophia Siu-chee Chan

Prof.

The University of Hong Kong

研究点 (4)

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