Pediatric Validation of CONOX Monitor During Surgery

NCT04826146 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 65

Last updated 2021-09-09

No results posted yet for this study

Summary

Pediatric Validation of CONOX Monitoring device (qCON and qNOX indices) for anesthesia depth during surgery

Conditions

  • Anesthesia
  • Anesthesia Awareness
  • Nociceptive Pain
  • Pediatric ALL
  • Surgery
  • Pain

Interventions

DEVICE

Validation of qCON versus BIS

Correlation between qCON and BIS values (main outcome) and qNOX and MOAA/S scale are determined

Sponsors & Collaborators

  • Patricio Gonzalez Pizarro

    lead OTHER

Eligibility

Min Age
1 Year
Max Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-07-01
Primary Completion
2021-12-01
Completion
2021-12-30
FDA Device
Yes

Countries

  • Spain

Study Locations

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Entities

Diseases

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 NCT04826146 on ClinicalTrials.gov