Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 4:37 PM
Ignite Modification Date: 2025-12-24 @ 4:37 PM
NCT ID: NCT06849466
Eligibility Criteria: Inclusion Criteria: 1. Adults aged 18-80 years, 2. Elective surgical patients scheduled for their first thoracoscopic lung resectiony, 3. ASA physical status I-III 4. sign the informed consent form Exclusion Criteria: 1. Severe heart failure or left ventricular ejection fraction (LVEF) \<30%, or the presence of coronary artery disease, cardiac conduction abnormalities, or arrhythmias; 2. Abnormal liver function, defined as ALT \>100 IU/L or Child-Pugh Class B; 3. Renal insufficiency, characterized by an estimated glomerular filtration rate (eGFR) \<60 mL/min or a preoperative serum creatinine level \>120 µmol/L; 4. A history of peptic ulcer disease, gastrointestinal bleeding, asthma, or cerebrovascular disease; 5. Known allergy to medications potentially used in this study, including dexmedetomidine, propofol, opioids, nonsteroidal anti-inflammatory drugs (NSAIDs), or local anesthetics; 6. Body mass index (BMI) \>30 kg/m²; 7. Preoperatively diagnosed psychiatric disorders, such as anxiety, depression, or sleep disturbances; 8. Long-term use of opioids or sedatives, defined as usage for 3 months or longer; 9. Pregnant women, postpartum individuals, and breastfeeding mothers; 10. Patients anticipated to require postoperative admission to the intensive care unit (ICU); 11. Patients with nasal abnormalities or conditions that preclude or contraindicate intranasal drug administration.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 80 Years
Study: NCT06849466
Study Brief:
Protocol Section: NCT06849466