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临床试验/NCT01547663
NCT01547663Unknown不适用

A Comparison of Pain Scales in Patients With Disorder of Consciousness Following Craniotomy

Mahidol University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2012年3月最近更新:
适应症

试验速览

阶段
不适用
入组人数
40
试验地点
1

研究概览

简要总结

This study aims to test validity, reliability and practicality of translated NCS, CNPI and FLACC in unconscious patients in 48 hour following craniotomy.

详细描述

This study aims to test predictive validity (sensitivity and specificity), content validity, concurrent validity, construct validity, inter-rater reliability and practicality of translated Nociception Coma Scale (NCS) , Checklist of Non Verbal Pain Indicator (CNPI) and the Faces, Legs, Activity, Cry, Consolability Observation Tool (FLACC) in unconscious patients in 48 hour following craniotomy.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age > 18 years old
  • Preoperative intracranial lesion which predicts delayed recovery
  • Disorder of consciousness within 48 hours after craniotomy assessed by using Coma Recovery Scale-Revised (CRS-R) 17
  • Not received postoperative sedation or muscle relaxants

排除标准

  • Documented history of prior brain injury
  • History of delayed development
  • Prior psychiatric illness
  • Prior neurological illness
  • Superior limb contusion, fracture, paralysis -cannot move
  • Thalamic hemorrhage -cannot express feeling

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Suwannee Suraseranivongse

Professor

Mahidol University

研究点 (1)

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