None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Adults age 19 and above ( no age limit for elderly ) 2) Patients with cardiogenic shock requiring intensive care monitoring in ICU 3) Patients elegible for oral medication administration 4) Patients who have provided research participation consent through a written informed consent form
Exclusion criteria
Exclusion criteria: 1) Unwilling or unable to obtain informed consent by the participant or substitute decision maker 2) Patients with acute coronary syndrome 3) Patients with severe valvular heart disease requiring emergent percutaneous procedures or surgery 4) Known hypersensitivity to beta-blockers 5) Patients with a history of bronchospasm or asthma 6) Patients with bradycardia or second or third-degree atrioventricular block 7) Patients with sick sinus syndrome, including sinoatrial block 8) Patients with untreated pheochromocytoma 9) Patients currently undergoing de-sensitization therapy 10) Patients who are currently pregnant, postpartum period within 30 days or breast-feeding
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 90-day all-cause mortality | — |
Secondary
| Measure | Time frame |
|---|---|
| All-cause mortality and cardiovascular mortality;Timing of discontinuation of inotropic or vasopressor agents;Pulmonary artery catheter monitoring parameters;The rate of Carvedilol intake on the 90th day;The target-dose achievement rate of Carvedilol on the 90th day;Heart failure rehospitalization rate;Follow-up echocardiography parameters;Complications related with pulmonary artery catheter | — |
Countries
Korea, Republic of
Contacts
Asan Medical Center