JPRN-jRCTs031210673招募中3 期
Ramelteon for prevention of postoperative delirium in delirium high-risk cancer patients.: A randomized, double-blind, placebo-controlled multi-center trial, JORTC-PON02/J-SUPPORT2103/NCCH2103. - RAMP trial
Matsuoka Hiromichi0 个研究点目标入组 766 人开始时间: 2022年4月1日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 发起方
- 入组人数
- 766
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 65age old 至 ot applicable(—)
- 性别
- All
入选标准
- •1) Pathologically confirmed and/or clinically suspected malignant tumor
- •2) Aged 65 or older at enrollment
- •3) Undergoing surgery under general anesthesia and postoperative hospitalization for 5 days or over
- •4) Preoperative ability to take medication orally or via nasogastric tube and postoperative plan to take medication orally or via nausal gastric tube from postoperative day 2 or earlier.
- •5) Written informed consent from patient or written informed consent from witness, who is not working in the present study, with patient's oral consent.
排除标准
- •1) Diagnosed as delirium with DSM-5 at enrollment
- •2) Allergy to ramelteon
- •3) Sevea liver dysfunction according to criteria of total bil > 2.25 mg/dL, AST > 90 U/L, ALT > 126 U/L for male, or ALT > 69 U/L for female
- •4) History of participation to clinical trials within 4 weeks including a day of enrollment except for the completed protocol treatment and in the observation period
- •5) History of medication of ramelteon or flurvoxamine within 2 weeks including a day of enrollment
- •6) History of medication of suvorexant or lemborexant 2 weeks including a day of enrollment
- •7) History of epilepsy, Parkinson's dosease, or dementia with lewy bodies
- •8) Lactose intolerance
- •9) Planned surgical procesure including central nervous system or intracranial region.
- •10) History of drug or alcohol use disorder or daily alcohol intake over 60g or alcohol-related disease within 5 years including a day of enrollment
- •11) History of participation to the present study
- •12) Comorbidity of moderate to severe dementia according to MMSE-J < 21
- •13) Severe visual or auditory handicap, or illiteracy
- •14) ECOG PS 4 at enrolment
- •15) Judgement as inadequate by principal investigator or other investigators
研究者
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