qCON/qNOX-Guided Anesthesia in Patients Undergoing Thyroidectomy Surgery
Recruiting
N/A
Interventional Study
Thyroid Surgeries
Intraoperative Analgesic Use
Anesthesia Depth Monitoring
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 – 70
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 90 (estimated)
- Sponsor
- Kayseri City Hospital · Government
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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.
Trial Locations
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Eligibility Criteria
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
Contacts