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 @ 5:01 PM
Ignite Modification Date: 2025-12-24 @ 5:01 PM
NCT ID: NCT01678950
Eligibility Criteria: Inclusion Criteria: * Patients equipped with a standard arterial catheter-line (femoral or radial artery) for invasive arterial blood pressure monitoring. * Patients requiring an echocardiographic evaluation - Transthoracic Echocardiographic Evaluation (TEE)or Transesophageal Echocardiographic Evaluation (TOE) - as a routine need or in the context of Acute Cardiocirculatory failure with suspected implication of cardiac dysfunction or Acute Respiratory failure and suspicion of cardiac failure. * \*When a pulmonary artery catheter (PAC, standard bolus thermodilution, ThD) is used or a central venous catheter linked with a femoral artery catheter to measure the transpulmonary thermodilution (PiCCO system: Continuous pulse contour cardiac analysis), the comparison will be done as a secondary end point of the protocol. * The point n.3 is optional Exclusion Criteria: * Related to MostCare: pathologies that could affect the quality and reliability of the arterial signal (aortic valve pathologies, aortic aneurysms) and arrhythmias that generate hemodynamic instability (i.e., variations in mean BP measurements \> 10%); poor quality of the arterial pressure signal after a standard flush test (i.e., over-damped or under-damped arterial trace). * Related to Echo-Doppler: non-feasibility to obtain a fulfilled quality of the images. * Patients younger than 18.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT01678950
Study Brief:
Protocol Section: NCT01678950