跳至主要内容
临床试验/NCT06364514
NCT06364514招募中不适用

PICNIC Study - PatIent Centered aNtIbiotic Courses in Children With Medical Complexity

Boston Children's Hospital1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2024年8月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
1
主要终点
Proportion of eligible patients who consent to participate in the intervention

研究概览

简要总结

To determine if clinicians can safely reduce antibiotic exposure in children with medical complexity (CMC) who are diagnosed with pneumonia by implementing an intervention that bases total antibiotic duration on an individual's clinical stability.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
2 Years 至 25 Years(Child, Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Admitted to the Complex Care Service at Boston Children's Hospital with a provider diagnosis of pneumonia
  • •Started on antibiotics by the provider team
  • •Ages 2-25 years old

排除标准

  • •Patients initially admitted to the intermediate care unit or ICU due to increased respiratory support needs

研究组 & 干预措施

Intervention Group

Experimental

Patients will be started on antibiotics for treatment of pneumonia per usual care by their medical provider team. The research team will monitor enrolled patients daily for markers of their clinical status (caregiver assessment of respiratory status, supplemental oxygen/respiratory support, presence of fever). Once the patient has been "clinically stable" x48 hours, antibiotics will be discontinued.

干预措施: Clinical Stability Assessment (Other)

结局指标

主要结局

Proportion of eligible patients who consent to participate in the intervention

时间窗: 48 hours

Caregiver and medical provider acceptability

Rate of persistent and worsening respiratory symptoms measured by patient's clinical status; the rate of emergency department revisit or hospital readmission within 1 week of antibiotic discontinuation

时间窗: 1 week

Patient Safety Outcomes

次要结局

  • Median days of antibiotics received for patients in the intervention group as well as from historical control group(30 days)

研究者

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

Kathleen Snow

Instructor, Pediatrics

Boston Children's Hospital

研究点 (1)

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