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临床试验/DRKS00013271
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Medication safety in patients treated with new oral anticancer agents: a prospective randomized investigation on the impact of intensified clinical pharmaceutical/clinical pharmacological care on patient safety and patient reported outcome - AMBORA

Apotheke des Universitätsklinikums Erlangen; Lehrstuhl für Klinische Pharmakologie und Klinische Toxikologie der FAU Erlangen-Nürnberg0 个研究点目标入组 202 人开始时间: 2017年11月3日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
202

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled study
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • Initiation of therapy with an oral anticancer agent, cancer diagnosis, adult patient, planned duration of therapy / estimated lifespan of at least 4 months, ability to complete questionnaires

排除标准

  • Prolonged inpatient stay and concomitant i.v. chemotherapy with classical cytostatic drugs, lack of german language skills, cognitive impairment, non-consenting patients, patients who are not able to take their medicine on their own, pregnant / lactating women, missing written consent

研究者

发起方
Apotheke des Universitätsklinikums Erlangen; Lehrstuhl für Klinische Pharmakologie und Klinische Toxikologie der FAU Erlangen-Nürnberg

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