qCON/qNOX-Guided Anesthesia in Patients Undergoing Thyroidectomy Surgery
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorKayseri City Hospital
About this trial
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.
Eligibility criteria
Qualifiers
Patients aged 18-70 years
Thyroidectomy cases with ASA physical status I-II
Patients who have provided written informed consent
Disqualifiers
Skin lesions preventing EEG electrode placement
Neurological disorders (e.g., epilepsy)
Anticipated difficult airway
Trial design
Treatments tested in this trial
- Connox EEG Monitoring
- standard anesthesia management
Treatment groups
90 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov