qCON/qNOX-Guided Anesthesia in Patients Undergoing Thyroidectomy Surgery
The aim of this study is to evaluate the effect of using the non-invasive Conox monitor on intraoperative opioid consumption. Additionally, the study aims to assess the impact of Conox monitoring on recovery time, postoperative agitation rate, and pain scores, and to investigate the correlation between qCON and qNOX va
| Condition(s) | Thyroid Surgeries, Intraoperative Analgesic Use, Anesthesia Depth Monitoring |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | The aim of this study is to evaluate the effect of using the non-invasive Conox monitor on intraoperative opioid consumption. Additionally, the study aims to assess the impact of Conox monitoring on recovery time, postoperative agitation rate, and pain scores, and to investigate the correlation between qCON and qNOX values and conventional hemodynamic parameters. |
| Who can participate | Inclusion Criteria: * Patients aged 18-70 years * Thyroidectomy cases with ASA physical status I-II * Patients who have provided written informed consent Exclusion Criteria: * Skin lesions preventing EEG electrode placement * Neurological disorders (e.g., epilepsy) * Anticipated difficult airway |
| Ages | 18 Years to 70 Years |
| Sex | All |
| Accepts healthy volunteers | Yes |
| Lead sponsor | Kayseri City Hospital |
| Locations | Kayseri, Kayseri, Turkey (Türkiye) |
| Start date | 2026-04-10 |
| NCT ID | NCT07445659 |
| Official listing | https://clinicaltrials.gov/study/NCT07445659 |