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

Conditions
Pain, Postoperative
Registration Number
NCT01547663
Lead Sponsor
Mahidol University
Brief Summary

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

Detailed Description

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.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
40
Inclusion Criteria
  1. Age > 18 years old
  2. Preoperative intracranial lesion which predicts delayed recovery
  3. Disorder of consciousness within 48 hours after craniotomy assessed by using Coma Recovery Scale-Revised (CRS-R) 17
  4. Not received postoperative sedation or muscle relaxants
Exclusion Criteria
  1. Documented history of prior brain injury
  2. History of delayed development
  3. Prior psychiatric illness
  4. Prior neurological illness
  5. Superior limb contusion, fracture, paralysis -cannot move
  6. Thalamic hemorrhage -cannot express feeling

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Siriraj Hospital, Mahidol University

🇹🇭

Bangkok, Thailand

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