Actively Recruiting
qCON/qNOX-Guided Anesthesia in Patients Undergoing Thyroidectomy Surgery
Led by Kayseri City Hospital · Updated on 2026-04-20
90
Participants Needed
1
Research Sites
11 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
qCON/qNOX-Guided Anesthesia in Patients Undergoing Thyroidectomy Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18-70 years
- Thyroidectomy cases with ASA physical status I-II
- Patients who have provided written informed consent
You will not qualify if you...
- Skin lesions preventing EEG electrode placement
- Neurological disorders (e.g., epilepsy)
- Anticipated difficult airway
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Kayseri City Hospital
Kayseri, Kayseri, Turkey (Türkiye), 38080
Actively Recruiting
Research Team
Ç
Çiğdem Ünal Kantekin, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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