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Clinical Trials/KCT0008687
KCT0008687
Recruiting
未知

A prospective observational study on the effectiveness of ANI and SPI as a measure of pain in patients undergoing cystoscopic procedure under remifentanil infusion

Inje University Sanggye Paik Hospital0 sites30 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Inje University Sanggye Paik Hospital
Enrollment
30
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Adult patients (\> 18 years) undergoing cystoscopic procedure under monitored anesthetic care (remifentanil infusion)

Exclusion Criteria

  • \- ASA physical status class 5
  • \- Morbid obesity ( BMI \=, \>35\)
  • \- Severe valvular heart disease
  • \- Arrhythmia such as atrial fibrillation
  • \- History of cardiac transplantation, Patients with cardiac pacemaker
  • \- CNS disorder, autonomic disease
  • \- Cognitive disorder including deliruim, dementia
  • \- Patients taking alpha\-2 agonist, beta blockers, or antiarrhythmics
  • \- Patients chronically taking sedative hypnotics and narcotic analgesics
  • \- Patients who underwent nerve block for pain control

Outcomes

Primary Outcomes

Not specified

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