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Intraoperative Nociception and Postoperative Pain

NCT03761433 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2019-07-12

No results posted yet for this study

Summary

If the individual patient's pain is assessed and the amount of analgesic needed after surgery is predicted, appropriate injection of pain control and excessive injection of narcotic analgesic can be prevented. Therefore, investigators try to evaluate the relation intraoperative nociception response with postoperative pain score.

In similar anesthetic depth(End tidal sevoflurane 3%) , changes of surgical pleth index values for stimulus of skin incision are thought to reflect the individual nociception characteristics.

Conditions

  • Pain, Postoperative
  • Nociceptive Pain
  • Analgesics

Interventions

DEVICE

SPI group

All patients applied surgical pleth index at the time of surgical incision, under End tidal Sevoflurane 3%

Sponsors & Collaborators

  • Samsung Medical Center

    lead OTHER

Eligibility

Min Age
20 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-11-30
Primary Completion
2019-05-20
Completion
2019-05-20

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03761433 on ClinicalTrials.gov