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临床试验/NCT03407404
NCT03407404终止2 期

Ketamine-Midazolam Versus Morphine-Midazolam for Continous Patient Sedation in Intensive Care Units in Uganda. A Randomised Controlled Trial.

Makerere University2 个研究点 分布在 1 个国家目标入组 124 人开始时间: 2017年10月22日最近更新:
适应症

试验速览

阶段
2 期
状态
终止
入组人数
124
试验地点
2
主要终点
incidence of hypotension

研究概览

简要总结

A prospective, double-blinded, multicenter randomized control trial. All critically ill patients above 12 years of age requiring continuous sedation for >24hrs in the ICU will be screened and those meeting selection criteria (and consented) will be enrolled into the study.

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详细描述

165 participants shall be consecutively randomized into either sedation with ketamine-midazolam or morphine-midazolam group using a block sequence technique; group concealed in brown envelopes. Blinding will be at patient/next of kin level as well as investigator/data collector level.

Enrolled subjects shall be followed up for treatment history, co-morbidities and related data will be collected, results analyzed and study findings will be availed to ICU physicians and Ministry of health to guide treatment considerations and for health care planning.

Data shall be collected using a standardized questionnaire by trained research assistants. It will be double entered into Epidata and exported to STATA version 12.0 for analysis. Continuous variables will be expressed as means and standard deviations, while categorical data will be expressed as frequencies with their respective percentages. Linear regression and logistic regression used to analyse primary outcomes, as well as multivariate analysis to detect associations.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

盲法说明

Drugs will be premixed and coded for ketamine-midazolam or morphine-midazolam. The colorless drug mixture shall be provided to the attending physician to start the infusion at 2ml/hour and to be titrated to the desired level of sedation.

The investigator and participant will be unaware of which group a certain patient is under.

入排标准

年龄范围
12 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age >12years of age.
  • Anticipated need for sedation for >24hours.

排除标准

  • Hypertensive crisis i.e. sustained SBP >200mmHg/DBP>110mmHg
  • Status epilepticus
  • Ischemic heart disease and severe LV dysfunction
  • Persistent tachyarrythmias
  • History of mental illness
  • Hypersensitivity to ketamine, morphine or midazolam.
  • Tetanus -due to the muscle rigidity that may be caused by ketamine. Reasons for exclusions 1 to 4; Ketamine stimulates the sympathetic nervous system causing transient increase in myocardial work and blood pressure and has psychoactive effects

结局指标

主要结局

incidence of hypotension

时间窗: 14 days

incidence of hypotension requiring vasopressor support.

duration of mechanical ventilation

时间窗: 14 days

in hours from start of mechanical ventialtion

incidence of delirium

时间窗: 14 days

assessed daily with the CAM-ICU score

次要结局

  • ICU length of stay(14 days)
  • mortality rate(within 14 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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