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Clinical Trial Summary

The purpose of this study is to evaluate the variations of respiratory changes in pulse oximeter plethysmographic amplitude (delta POP) according to different contact forces between finger and sensor of pulse oximeter. During general anesthesia without surgical stimuli, pulse oximeter sensor is applied with serial contact force, from 0 to maximal 1.5N (increased by 0.2N) and POP waveform is obtained for 60 seconds. Delta POP will be calculated and compared.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Children Under General Anesthesia

NCT number NCT02940938
Study type Interventional
Source Seoul National University Hospital
Contact Hee-Soo Kim, MD, PhD
Email dami0605@snu.ac.kr
Status Recruiting
Phase N/A
Start date January 2017
Completion date December 2017

See also
  Status Clinical Trial Phase
Completed NCT01411020 - Target-controlled Infusion of Propofol for Induction of Pediatric Anesthesia Phase 4