Clinical trial · Observational
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
NCT04826146CI-TRIAL-00053800unknownClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Pediatric Validation of CONOX Monitoring device (qCON and qNOX indices) for anesthesia depth during surgery
Conditions
Conditions (6)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Anesthesia | — | UNRESOLVED | — |
| Anesthesia Awareness | — | UNRESOLVED | — |
| Nociceptive Pain | — | UNRESOLVED | — |
| Pain | — | UNRESOLVED | — |
| Pediatric ALL | Childhood Acute Lymphoblastic Leukemia | ALIAS | 0.90 |
| Surgery | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Validation of qCON versus BIS | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- CONOX
- description
- Patients are monitored with BIS and CONOX
- interventionNames
- Device: Validation of qCON versus BIS
Primary outcomes (1)
- measure
- Correlation of qCOX and BIS values
- timeFrame
- prospective data acquisition through study completion, an average of 1 year
- description
- Both values are correlated by a blind investigator
Secondary outcomes (1)
- measure
- Correlation of qNOX and MOAA/S values
- timeFrame
- prospective data acquisition through study completion, an average of 1 year
- description
- Both values are correlated by a blind investigator
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 1 Year
- Maximum age
- 18 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available
No reference posted for this study.