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:
2025-12-26 @ 2:39 PM
Ignite Modification Date:
2025-12-26 @ 2:39 PM
NCT ID:
NCT00988806
Eligibility Criteria:
Inclusion Criteria:
* Age over 18
* Severe symptoms of heart failure with dyspnea and/or fatigue at rest or minimal effort (functional class III and IV of NYHA)
* Episodes of fluid retention (pulmonary or systemic venous congestion, peripheral edema) and/or low cardiac output at rest (peripheral hypoperfusion)
* objective evidence of severe cardiac dysfunction determined by the presence of at least one of the following:
* Left ventricular ejection fraction \</= 30%
* A severe impairment of cardiac function by echocardiography with Doppler transmitral flow pattern pseudonormal or restrictive.
* A left ventricular filling pressure elevated (PCP\> 16 mmHg and / or DBP average\> 12 mm Hg for pulmonary artery catheterization)
* Levels of BNP or NT-proBNP higher in the absence of noncardiac causes for this.
* Severe impairment of functional capacity as evidenced by one of the following:
* Inability to exercise
* A distance \<300 m or less in women and / or patients \>/= 75 years in the 6-minute walk test
* A test of myocardial oxygen consumption \<12-14 ml / kg / min.
* \>/= 1 prior history of HF hospitalization in the previous 6 months
* Presence of all the above criteria despite attempts to optimize therapy including diuretics, inhibitors of the renin-angiotensin-aldosterone system and beta-blockers, unless these drugs were not tolerated or were contraindicated, and cardiac resynchronization therapy when indicated.
* consent to participate in the study.
Exclusion Criteria:
* Levosimendan allergy or hypersensitivity.
* Severe renal impairment (creatinine clearance \<30 ml / min).
* Severe liver impairment.
* History of autoimmune disease.
* Pregnancy.
* Women of childbearing age not using adequate contraception (hormonal, IUD, barrier + spermicide)
* Heart disease with significant obstructions to ventricular filling or emptying.
* Severe hypotension (Systolic \< 90 mmHg).
* Tachycardia \> 120 bpm or a history of torsion point type ventricular tachycardia.
* Severe concomitant disease with decreased short-term prognosis.
* Inability to give informed consent.
* Participation in another study.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00988806
Study Brief:
Protocol Section:
NCT00988806