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 @ 5:38 PM
Ignite Modification Date:
2025-12-24 @ 5:38 PM
NCT ID:
NCT03412968
Eligibility Criteria:
Inclusion Criteria:
* Patients who signed informed consent
* Patients not undergoing emergency surgery.
* Surgical procedures performed under normothermic conditions.
* Patients with a minimum time of 40 minutes before decannulation (after the end of myocardial reperfusion, unclamping of the aorta and the end of CPB).
Exclusion Criteria:
* Emergency medical condition in which it is not possible to collect study data.
* Heart condition requiring the use of hypothermia or hyperthermia during CPB.
* Patients without a minimum time of 40 minutes before decannulation (after the end of myocardial reperfusion, unclamping of the aorta and the end of CPB).
* Patients who cannot manage their fluid balance on their own through diuresis prior to CPB.
* Patients who are unable to manage excess volume during the surgical procedure by means of spontaneous or forced diuresis with diuretics (positive cumulative balance despite intravenous bolus of diuretics after 75% of the anticipated duration of CPB according to the course of the surgery).
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT03412968
Study Brief:
Protocol Section:
NCT03412968