Pediatric Validation of CONOX Monitor During Surgery

Monitoring the Depth of Anesthesia Using the qCON and qNOX Indices During Pediatric Surgery: a Multi-centre Study

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT04826146

Enrollment

Registered

2021-04-01

Start date

2020-07-01

Completion date

2021-12-30

Last updated

2021-09-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia, Anesthesia Awareness, Nociceptive Pain, Pain, Pediatric ALL, Surgery

Brief summary

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

Interventions

DEVICEValidation of qCON versus BIS

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

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

1 Years to 18 Years

Healthy volunteers

Yes

Inclusion criteria

* General Anesthesia using propofol, sevoflurane or desflurane * ASA I - IV * Surgical procedure longer than 60 minutes

Exclusion criteria

* Neurological disorders * Inability to correctly place BIS and CONOX probes in forehead * Pregnancy * Active prescription for drugs involving chronic pain and / or central nervous system * Hemodynamic instability

Design outcomes

Primary

Measure	Time frame	Description
Correlation of qCOX and BIS values	prospective data acquisition through study completion, an average of 1 year	Both values are correlated by a blind investigator

Secondary

Measure	Time frame	Description
Correlation of qNOX and MOAA/S values	prospective data acquisition through study completion, an average of 1 year	Both values are correlated by a blind investigator

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026