RECRUITINGINTERVENTIONAL
Pulmonary Artery Catheterization and Carvedilol Early Initiation in Cardiogenic SHOCK Due to HFrEF
Pulmonary Artery Catheterization and Carvedilol Early Initiation in Cardiogenic SHOCK Caused by Heart Failure With Reduced Ejection Fraction
About This Trial
This study aims to compare the impact of hemodynamic monitoring using pulmonary artery catheter (PAC) on survival and inotropic agent reduction in patients with cardiogenic shock caused by heart failure with reduced ejection fraction (HFrEF). The investigators also intend to compare the difference in long-term survival rates among patients who have recovered from cardiogenic shock due to HFrEF, based on the timing of initiation of beta-blocker treatment.
Who May Be Eligible (Plain English)
Who May Qualify:
- Adults age 19 and above ( no age limit for elderly )
- Patients with cardiogenic shock requiring intensive care monitoring in ICU
- Patients eligible for oral medication administration
- Patients who have provided research participation consent through a written willing to sign a consent form form
Who Should NOT Join This Trial:
- Unwilling or unable to obtain willing to sign a consent form by the participant or substitute decision maker
- Patients with mechanical circulatory support at the time of screening
- Patients with acute coronary syndrome
- Patients with severe valvular heart disease requiring emergent percutaneous procedures or surgery
- Known hypersensitivity to beta-blockers
- Patients with a history of bronchospasm or asthma
- Patients with bradycardia or second or third-degree atrioventricular block
- Patients with sick sinus syndrome, including sinoatrial block
- Patients with untreated pheochromocytoma
- Patients currently undergoing de-sensitization therapy
- Patients who are currently pregnant, postpartum period within 30 days or breast-feeding
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
* Adults age 19 and above ( no age limit for elderly )
* Patients with cardiogenic shock requiring intensive care monitoring in ICU
* Patients eligible for oral medication administration
* Patients who have provided research participation consent through a written informed consent form
Exclusion Criteria:
* Unwilling or unable to obtain informed consent by the participant or substitute decision maker
* Patients with mechanical circulatory support at the time of screening
* Patients with acute coronary syndrome
* Patients with severe valvular heart disease requiring emergent percutaneous procedures or surgery
* Known hypersensitivity to beta-blockers
* Patients with a history of bronchospasm or asthma
* Patients with bradycardia or second or third-degree atrioventricular block
* Patients with sick sinus syndrome, including sinoatrial block
* Patients with untreated pheochromocytoma
* Patients currently undergoing de-sensitization therapy
* Patients who are currently pregnant, postpartum period within 30 days or breast-feeding
Treatments Being Tested
DEVICE
Pulmonary artery catheter
Pulmonary artery catheter monitoring or not
Locations (1)
Asan Medical Center
Seoul, South Korea