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A study of analgesic nociception index-guided requiring a dose of remifentanil during mechanical ventilatory support under continuous sedation in the intensive care unit

Not Applicable
Conditions
Postoperative patients required mechanical ventilatory support under continuous sedation in the intensive care unit
Registration Number
JPRN-UMIN000051696
Lead Sponsor
Ehime university
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
60
Inclusion Criteria

Not provided

Exclusion Criteria

Patients are 18 years old or less, underwent previous cardiac surgery, have severe arrhythmia, atrial fibrillation, and an implanted pacemaker, require high doses of catecholamines, or take some opioid medications preoperatively.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The total dose of remifentanil administered between admission to the intensive care unit and the next morning
Secondary Outcome Measures
NameTimeMethod
The mean score of HFVI, Total dose of sedative agents, The frequency of analgesics required after the termination of mechanical ventilatory support, VAS sore after the termination of mechanical ventilatory support, The development of delirium after the termination of mechanical ventilatory support, The cut-off value of HFVI score for BPS >5
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