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Clinical Trials/NCT04727073
NCT04727073
Terminated
Phase 3

Spironolactone in the Treatment of Heart Failure- a Double-blind, Randomized, Placebo-controlled, Parallel Group Interventional Phase III Study to Determine Efficacy and Safety of Spironolactone on the Composite Endpoint of Recurrent Heart Failure Hospitalizations and Cardiovascular Death in Patients with Heart Failure with Mid-range or Preserved Ejection Fraction

Charite University, Berlin, Germany69 sites in 3 countries743 target enrollmentNovember 1, 2018

Overview

Phase
Phase 3
Intervention
Placebo Comparator
Conditions
Not specified
Sponsor
Charite University, Berlin, Germany
Enrollment
743
Locations
69
Primary Endpoint
Primary Objective: Cumulative number of primary composite events of cardiovascular (CV) death and total HF hospitalizations
Status
Terminated
Last Updated
last year

Overview

Brief Summary

The purpose of this study is to determine whether the treatment of patients with HFmrEF and HFpEF at high risk of cardiovascular events with the mineralocorticoid receptor antagonist (MRA) spironolactone reduces a composite of recurrent heart failure hospitalizations and cardiovascular mortality.

Detailed Description

The primary objective of the SPIRIT-HF study is to compare Spironolactone to Placebo in reducing the rate of the composite endpoint of recurrent heart failure hospitalizations and cardiovascular (CV) death in symptomatic HF patients (NYHA II-IV) with mid-range (LVEF 40- 49 %) or preserved (LVEF ≥ 50 %) ejection fraction. The efficacy and safety of mineralocorticoid receptor antagonist (MRA) in reducing the risk of death and hospitalizations has been proven with two separate substances (Spironolactone; RALES 1999 and Eplerenone; EMPHASIS 2011) in symptomatic heart failure patients with reduced left- ventricular ejection fraction (HFrEF). In 2013 the TOPCAT investigators tried to proof similar efficacy in patients with heart failure and preserved ejection fraction (≥ 45%). Because of regional variations in the enrollment process and difficulties regarding drug adherence the trial revealed neutral findings but the substance spironolactone was still able to show its potential benefit in the American cohort. Hence, the investigators see a strong rationale for testing a mineralocorticoid receptor blocker in patients suffering from heart failure with mid-range or preserved left ventricular ejection fraction. Intervention: Mineralocorticoid receptor blocker Spironolactone in tablet form taken daily. Starting dosage will be 25 mg OD with dosage escalation to 50 mg OD within 4 weeks if kidney function at VR was \> 30 mL/min/m2 and potassium \< 4.5 mmol/L. Spironolactone is not approved for the treatment of HFmrEF and HFpEF. Matching placebo in tablet form taken daily with dosage escalation rules in accordance with dosage of the study drug Spironolactone. Visits: Screening (VScr), Visit of Randomization (VR), V1 Safety Visit (1 week), V2 (4 weeks), V2S Safety Visit (5 week), V3 (4 months), V4 (8 months), V5 (12 months), V6 (18 months), V7 (24 months), V8 (30 months), V9 (36 months), V10 (42 months), V11/EOT (48 months); VXS (1 week after Visit X). Individual intervention duration with spironolactone or placebo will be continued until the overall expected event rate is reached or until withdrawal of informed consent. Based on previous HF trials the investigators calculate a mean follow-up duration of 3 years (range 2-4 years) depending on the individual inclusion date. Duration of follow-up will be event-rate based, with an expected overall study duration of 60 months. With an anticipated recruitment phase of 24 months; this will result in a maximum follow-up of 48 months and an average follow-up per patient of 36 months assuming a constant recruitment rate.

Registry
clinicaltrials.gov
Start Date
November 1, 2018
End Date
October 1, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Univ.-Prof. Dr. med. Frank Edelmann

Univ. Prof. Dr. med. Frank Edelmann

Charite University, Berlin, Germany

Eligibility Criteria

Inclusion Criteria

  • Patients eligible for inclusion in this study have to fulfill all of the following criteria:
  • Written informed consent.
  • Male or female, age ≥ 50 years
  • Current symptoms of Heart Failure (NYHA ≥ II) during VR
  • Symptom(s) of HF ≥ 30 days prior to VR
  • HF Hospitalization or treatment with intravenous (IV) diuretics for worsening HF within 12 months prior to VR
  • Left ventricular ejection fraction ≥ 40 % at screening measured by echocardiography and evidence of structural/ functional abnormalities (at least one of the following criteria): LAVI \> 34 ml/m2// E/émean ≥ 13// Mean e' (septal and lateral) \< 9 cm/s
  • NT-proBNP \> 300 pg/ml (SR) or \> 900 pg/ml (AF) on the Visit 1 ECG; only if NT-proBNP is NOT available: BNP \> 80/ 250 pg/ml (SR/AF)
  • Controlled systolic BP: defined as a target systolic BP \< 140 mm Hg. Subjects with BP up to and including 160 mm Hg are eligible for enrollment if on 3 or more medications to control BP (Patients with uncontrolled BP should be considered for Re-Screening after optimization of antihypertensive therapy has been established)
  • Serum potassium \< 5.0 mmol/L prior to randomization

Exclusion Criteria

  • Patients fulfilling any of the following criteria are not eligible for inclusion in this study. The investigator may apply no additional exclusion criteria, in order to ensure that the study population will be representative of all eligible patients.
  • Hyperkalemia (potassium level ≥ 5.5 mmol/L) within the past two weeks before VR
  • Hyponatraemia (sodium level \< 135 mmol/L) prior to randomization
  • Severe renal dysfunction, defined as an estimated glomerular filtration rate of less than 30 mL/min/1.73m2) as calculated by the Modification in Diet in Renal Disease (MDRD) formula at Visit 1 or serum creatinine level ≥ 1,8 mg/dl (\> 160 μmol/ml)
  • History of anuria or acute renal failure (as defined by the RIFLE criteria for AKI; see Appendix XVIII.3) within the past two weeks before VRenal dysfunction, defined as an estimated glomerular filtration rate of less than 30 mL/min/1.73m2) as calculated by the Modification in Diet in Renal Disease (MDRD) formula at VScr/VR or serum creatinine level ≥ 1,8 mg/dl (\> 160 μmol/ml)History of anuria or acute renal failure (as defined by the RIFLE criteria for AKI; see Appendix XVIII.3) within the past two weeks prior to randomization
  • Acute coronary syndrome (including MI) and elective PCI within 30 days prior to VR.
  • Cardiac surgery, other major CV surgery, or urgent percutaneous coronary intervention (PCI) within the 3 months prior to VR
  • Current acute decompensated HF requiring augmented therapy with i.v. diuretics, i.v. vasodilators and/or i.v. inotropic drugs. Patients are eligible after initial stabilization.
  • Probable alternative diagnoses that in the opinion of the investigator could account for the patient's HF symptoms (i.e., dyspnea, fatigue) such as significant pulmonary disease (including primary pulmonary HTN), anemia or obesity. Specifically, patients with the following are not eligible for randomization:
  • Severe pulmonary disease including chronic obstructive pulmonary disease (COPD) or severe asthma bronchiale ( (ie requiring home oxygen, chronic nebulizer therapy, chronic oral steroid therapy) or

Arms & Interventions

Arm B

Placebo Comparator: Placebo Placebo of Spironolactone in tablet form taken daily with dosage escalation rules in accordance with dosage of the study drug Spironolactone.

Intervention: Placebo Comparator

Outcomes

Primary Outcomes

Primary Objective: Cumulative number of primary composite events of cardiovascular (CV) death and total HF hospitalizations

Time Frame: Time Frame: Total follow up time (up to 48 months)

Cumulative number of primary composite events of cardiovascular (CV) death and total (first and recurrent) HF hospitalizations in symptomatic HF patients (NYHA II-IV) with mid-range (LVEF 40- 49 %) or preserved (LVEF ≥ 50 %) ejection fraction.

Secondary Outcomes

  • Secondary Objective: Comparison of spironolactone to placebo in reducing the rate of hospitalisations and deaths(Time Frame: Total follow up time (up to 48 months))

Study Sites (69)

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