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:
2026-03-26 @ 3:15 PM
Ignite Modification Date:
2026-03-26 @ 3:15 PM
NCT ID:
NCT07335250
Eligibility Criteria:
Inclusion Criteria:
* Provision of written informed consent
Age between 18 and 85 years
ASA Physical Status classification I-III
Elective thoracotomy with planned unilateral lobectomy
Anticipated hospital stay of at least one night
Expected requirement for parenteral opioid analgesia for at least 24 hours postoperatively
Ability to operate an intravenous patient-controlled analgesia (PCA) device
Exclusion Criteria:
* Patients undergoing emergency surgery
Presence of infection or open wound at the injection site
Coagulopathy
Hepatic or renal failure
Patients undergoing reoperation
Patients with missing or incomplete data
Pregnancy or lactation
Tracheal malformation or tracheostomy
Chronic opioid use (≥30 days within the last 3 months, ≥15 mg/day morphine equivalent)
Patients exceeding the maximum safe local anesthetic dose based on weight (2.5 mg/kg, max 150 mg)
Patients who refuse data privacy consent will be excluded from the study
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
85 Years
Study:
NCT07335250
Study Brief:
Protocol Section:
NCT07335250