Pediatric Validation of CONOX Monitor During Surgery

Patricio Gonzalez Pizarro

Status: Unknown

Conditions: Surgery; Nociceptive Pain; Pediatric ALL; Anesthesia Awareness; Pain; Anesthesia

Treatments: Device: Validation of qCON versus BIS

Study type: Observational

Funder types: Other

Identifiers

NCT04826146

PI-3871

Details and patient eligibility

About

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

Enrollment: 65 estimated patients

Sex: All

Ages: 1 to 18 years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

65 participants in 1 patient group

CONOX

Description:

Patients are monitored with BIS and CONOX

Treatment:

Device: Validation of qCON versus BIS