Comparative Study of Adherence to Antibiotic Therapy Among Pediatric Patients: Hospital Emergency Department vs. Primary Care Center (ObsATBGignaUrg)
2026年7月13日 更新者：University Hospital, Montpellier
Comparative Study of Adherence to Antibiotic Therapy Among Pediatric Patients: The Gignac Primary Care Medical Center Versus the Pediatric Emergency Department of Montpellier University Hospital (CHU Montpellier).
This study was initiated because of the limited litterature available on this topic.
The objective was to compare adherence to antibiotic therapy among a pediatric population treated in two healthcare settings in France: the Gignac Health Center, a primary care facility, and the Pediatric Emergency Department of Montpellier University Hospital.
This observational study assessed treatment adherence through a telephone questionnaire administered to parents after the theorical end of the treatment.
研究概览
研究类型
观察性的
注册 (估计的)
191
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习联系方式
- 姓名：Eric E JEZIORSKI, Professor of Medicine
- 电话号码：+33627383451
- 邮箱：e-jeziorski@chu-montpellier.fr
参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 孩子
接受健康志愿者
不
取样方法
非概率样本
研究人群
Pediatric patients presenting to the Gignac Primary Care Health Center or the Pediatric Emergency Department of Montpellier University Hospital with a suspected bacterial infection and considered eligible for an outpatient oral antibiotic prescription.
描述
Inclusion Criteria:
- Children aged 3 months to 16 years
- Receiving an outpatient oral antibiotic prescription
- Diagnosed with an acute bacterial infection
Exclusion Criteria:
- Unemancipated minors presenting without a parent or legal guardian.
- Participation in another clinical research study with an ongoing exclusion period
- Refusal to participate after the reflection period
- Parents unable to understand the study information (e.g., language barrier or cognitive impairment)
- Not affiliated with, or not a beneficiary of, a national health insurance scheme
- Pregnant or breastfeeding female participants
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
队列和干预
团体/队列 |
|---|
|
Pediatric patients prescribed antibiotic for acute bacterial infection at the Gignac Health center
Pediatric patients aged 3 months to 16 years presenting with an acute bacterial infection and prescribed an outpatient antibiotic treatment were eligible for inclusion.
Parents were contacted by telephone between 15 and 21 days after the antibiotic prescription to assess treatment adherence.
|
|
Children prescribed antibiotic for acute bacterial infection at pediatric emergency of Montpellier
Pediatric patients aged 3 months to 16 years presenting with an acute bacterial infection at pediatric emergency department Montpellier University Hospital and prescribed an outpatient antibiotic treatment were eligible for inclusion.
Parents were contacted by telephone between 15 and 21 days after the antibiotic prescription to assess treatment adherence.
|
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Proportion of patients who adhered to the antibiotic prescription provided by the general practitioner (GP) or the emergency physician (University Hospital)
大体时间：The study period extended from the initial consultation (antibiotic prescription) to 21 days after the prescription, depending on the prescribed treatment duration.
|
Treatment adherence was considered satisfactory when at least 80% of the prescribed antibiotic course was taken
|
The study period extended from the initial consultation (antibiotic prescription) to 21 days after the prescription, depending on the prescribed treatment duration.
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 研究主任：Eric E JEZIORSKI, Professor of Medicine at Montp、Pediatric Emergency Department, Montpellier University Hospital
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年9月1日
初级完成 (估计的)
2028年8月1日
研究完成 (估计的)
2028年9月1日
研究注册日期
首次提交
2026年7月13日
首先提交符合 QC 标准的
2026年7月13日
首次发布 (实际的)
2026年7月17日
研究记录更新
最后更新发布 (实际的)
2026年7月17日
上次提交的符合 QC 标准的更新
2026年7月13日
最后验证
2026年7月1日
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- RECHMPL25_0564
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)？
不
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.