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:
2025-12-25 @ 3:14 AM
Ignite Modification Date:
2025-12-25 @ 3:14 AM
NCT ID:
NCT05691205
Eligibility Criteria:
Inclusion Criteria:
* Recipient of LUTX
* Age \> 18 years
* Signed informed consent
Exclusion Criteria:
* Age \< 18 years
* Already undergone LUTX
* Major hemodynamic instability along the 24 hours following LUTX: systolic arterial pressure \< 90 mmHg and/or heart rate \> 120 beat/min and/or high dose vasopressor requirement (norepinephrine \> 0.3 mcg/kg/min and/or epinephrine \> 0.2 mcg/kg/min and/or dobutamine \> 8mcg/kg/min)
* Documented post-LUTX endobronchial plasma leak requiring high levels of PEEP \> 15 cmH2O
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT05691205
Study Brief:
Protocol Section:
NCT05691205