Pragmatic Randomized Controlled Trial of Electronic Health Record-based Reminder System to Measure Serum Lithium Levels among Patients with Mood Disorder - Kyoto tOyooka Nested cOntrolled Trial Of RemInders (KONOTORI) Study

Graduate School of Medicine and Public Health, Kyoto University0 个研究点目标入组 111 人开始时间: 2018年10月1日最近更新: 2023年10月17日

适应症

试验速览

阶段: 未知
状态: 已完成
发起方
入组人数: 111

研究概览入排标准研究者记录与标识符相似试验

研究概览

简要总结

At the follow-up, the difference in the primary outcome (the achievement of therapeutically appropriate serum lithium levels between 0.4 and 1.0 mEq/L at 18 months after enrollment) was not statistically significant between the reminder group and the usual care group. The median number of serum lithium monitoring was significantly higher in the reminder group than in the usual care group. The exacerbation of mood disorders was similar between two groups.

研究设计

研究类型: Interventional

入排标准

年龄范围: 18years-old 至 ot applicable（—）
性别: All

入选标准

未提供

排除标准

•1) Prescribed lithium for a condition other than mood disorder 2) Who did not provide written informed consent 3) Schizophrenia 4) Inappropriate/unable to participate in the trial (as judged by treating psychiatrist) 5) Serious suicide intent (as judged by treating psychiatrist) 6) Lithium intoxication 7) Pregnancy 8) Researcher of the trial and their family 9) Who cannot read Japanese 10) Contraindication of lithium 11) Participation in another clinical trial 12) Inpatients 13) End-stage physical disease 14) Who did not have serum lithium level measurement at baseline 15) Who did not visit hospital between 4-8 months after inclusion

研究者

发起方

Graduate School of Medicine and Public Health, Kyoto University

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