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 @ 9:26 PM
Ignite Modification Date: 2025-12-24 @ 9:26 PM
NCT ID: NCT01298232
Eligibility Criteria: Inclusion Criteria: 1. Patients who are hospitalized due to AHFS and have a plasma NT-proBNP ≥ 1600 pg/ml at admission. 2. Patients give written consents to participate in the study. Exclusion Criteria: 1. Patients with an implanted pacemaker. 2. Patients with chronic kidney disease, stage 5 and warranted dialysis. 3. Patients with hypertrophic obstructive cardiomyopathy. 4. Patients with cardiac temponade or constrictive pericarditis. 5. Acute coronary syndrome, stroke, transient ischemic attack, cardiac, carotid or major vascular surgery, percutaneous coronary intervention (PCI) or carotid angioplasty, within the past 1 months prior to index hospitalization. 6. Coronary or carotid artery disease likely to require surgical or percutaneous intervention within the 6 months after discharge at index hospitalization. 7. Patients with left ventricular assistance device (LVAD device). 8. Documented ventricular arrhythmia with syncope episodes within past 3 months, prior to index hospitalization that is untreated. 9. Symptomatic bradycardia or second or third degree heart block without a pacemaker. 10. Implantation of a CRT (cardiac resynchronization therapy) device within the prior 1 month before index hospitalization or intent to implant a CRT device. 11. Presence of hemodynamically significant mitral and/or aortic valve disease, except mitral regurgitation secondary to left ventricular dilatation. 12. Presence of other hemodynamically significant obstructive lesions of left ventricular outflow tract, including aortic and sub-aortic stenosis. 13. Severe primary pulmonary, renal or hepatic disease. 14. Presence of any other disease with a life expectancy of \< 1 year. 15. Subjects get pregnant or will be pregnant within 1 month.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT01298232
Study Brief:
Protocol Section: NCT01298232