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: 2025-12-25 @ 2:15 AM
Ignite Modification Date: 2025-12-25 @ 2:15 AM
NCT ID: NCT06285760
Eligibility Criteria: Inclusion Criteria: * Patients admitted for acute heart failure and ≥ 1 clinical sign of volume overload (edema, ascites, or pleural effusion). * NTproBNP levels \>1000 pg/mL or BNP \>250 ng/mL on admission. * Under treatment with furosemide and iSGLT2 according to European guidelines and indication of association of another diuretic due to residual congestion data defined by ADVOR SCORE\>1. Exclusion Criteria: * Systolic blood pressure \<90 mmHg or mean arterial pressure \< 65 mmHg. * Maintenance treatment with acetazolamide/ Treatment with acetazolamide in the month prior to inclusion in the study. * Anticipated need for intravenous inotropes, vasopressors or nitroprusside during the study. * Contraindication to ISGLT2. * Type 1 diabetes mellitus * GFR \< 20 ml/min/m2 or renal replacement therapy/ultrafiltration at any time prior to the study. * Anticipated exposure to nephrotoxic agents, such as iodinated contrast during admission. * Concurrent diagnosis of acute coronary syndrome. * History of congenital heart disease requiring surgical correction. * History of cardiac transplantation and/or ventricular assist device. * Pregnant or breastfeeding patients. * Inability to adequately collect diuresis. * Serum potassium less than 3.5 mEq/L. * Venous pH \<7.30 * Severe aortic stenosis or obstructive hypertrophic cardiomyopathy. * Sulfonamide allergy, liver cirrhosis, renal lithiasis.
Healthy Volunteers: False
Sex: ALL
Study: NCT06285760
Study Brief:
Protocol Section: NCT06285760