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Validation of Pupillary Response to Nociceptive Stimulation in Cardiac Surgery During Extracorporeal Circulation Period

NCT03568396 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2019-02-27

No results posted yet for this study

Summary

The relationship between the target effect site concentration of remifentanil and the pupil diameter and reactivity in response to a standard noxious stimulus in cardiac surgery during extra corporeal circulation will be evaluated.

Conditions

  • Pupil
  • Analgesics
  • Opioid Use
  • Dose-Response Relationship, Drug
  • Anesthetics, Intravenous
  • Surgery, Cardiac
  • Circulation, Extracorporeal
  • Electric Stimulation
  • Electroencephalography/Drug Effects
  • Monitoring, Intraoperative
  • Adult
  • Remifentanil

Interventions

DEVICE

Pupillometer

Measurement of pupil diameter and reactivity in response to a standard noxious stimulus in cardiac surgery during extracorporeal circulation period.

Sponsors & Collaborators

  • University Hospital, Tours

    lead OTHER

Principal Investigators

  • Fabien ESPITALIER, M.D · University Hospital, Tours

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-08-22
Primary Completion
2018-10-25
Completion
2018-10-25

Countries

  • France

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 NCT03568396 on ClinicalTrials.gov