NCT02413957已完成不适用
Pilot Project to Investigate the Influence of Medication Reconciliation and an Extensive Medication Safety Check on the Number of Adverse Drug Events in the Elderly
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 220
- 试验地点
- 1
- 主要终点
- incidence of adverse drug events
研究概览
简要总结
The purpose of this study is to determine wether an extensive medication safety check has a greater impact on the incidence of adverse drug events than medication reconciliation or no intervention.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Health Services Research
- 盲法
- None
入排标准
- 年龄范围
- 65 Years 至 —（Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patient 65 years and older
- •written informed consent patient or the legal representative
- •existing medication therapy at hospitalization
- •admission to one of the project wards via emergency department (non elective)
排除标准
- •- patients included in the study previously
研究组 & 干预措施
Controll-Group
No Intervention
Patient randomized to the Control-Group will receive the traditional care by physician and nurse on the ward.
MedRec-Group
Experimental
Patient randomized to the MedRec-Group will receive the traditional care by physician and nurse on the ward and additional pharmacist led medication reconciliation.
干预措施: Medication Reconciliation (Other)
AMTS-Group
Experimental
Patient randomized to the AMTS-Group will receive the traditional care by physician and nurse on the ward and additional pharmaceutical care by a pharmacist.
干预措施: Pharmaceutical Care (Other)
结局指标
主要结局
incidence of adverse drug events
时间窗: 1 year
次要结局
- Assessment of the clinical relevance of medication related problems as determined by the French Society of Clinical Pharmacy(1 year)
- Assessment of the clinical relevance of discrepancies as determined by the French Society of Clinical Pharmacy(1 year)
- number of medication related problems(1 year)
- number of discrepancies(1 year)
- duration of taking the best possible medication history(1 year)
研究者
研究点 (1)
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