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NCT04023227CompletedPhase 4

Efficacy and Safety of Sacubitril/Valsartan Compared With Enalapril on Morbidity, Mortality, and NT-proBNP Change in Patients With CCC

A Multicenter, Prospective, Randomized, Open-label, Blinded-endpoint, Phase 4 Study to Evaluate the Efficacy and Safety of Sacubitril/Valsartan Compared With Enalapril on Morbidity, Mortality, and NT-proBNP Change in Patients With Chronic Chagas' Cardiomyopathy. The Study is Also Know as Prevention And Reduction of Adverse Outcomes in Chagasic Heart failUre Trial Evaluation (PARACHUTE-HF).

Source: ClinicalTrials.gov · Last updated 11 May 2026

Brief summary (registry, in English)

The purpose of this study was to evaluate the effect of sacubitril/valsartan 200 mg BID compared with enalapril 10 mg BID, in addition to conventional heart failure (HF) treatment, in improving a hierarchical composite of cardiovascular (CV) events (i.e. CV death or the occurrence of first HF hospitalization) and causing a greater reduction in n terminal prohormone of brain natriuretic peptide (NT-proBNP, at Week 12 from Baseline) in participants with HF with reduced ejection fraction (HFrEF) caused by chronic Chagas' cardiomyopathy (CCC).

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
922 (actual)
First submitted
10 Jul 2019
Start date
10 Dec 2019
Primary completion date
16 Mar 2025
Lead sponsor
Novartis Pharmaceuticals
NCT number
NCT04023227

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 922
  • From 10 Dec 2019 to the primary completion date, 16 Mar 2025
  • 54 sites in 4 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Presence of other cardiac conditions:
    • Previous cardiac surgery
    • Heart failure where, in the Investigator's judgement, there is a possible alternative primary etiology e.g., due to coronary artery disease, valve disease, congenital heart disease or other causes.
    • Untreated arrhythmia or serious conduction disease e.g., bradyarrhythmias, atrial fibrillation with rapid ventricular response, second or third degree atrioventricular block, etc.
    • Primary uncorrected valvar pathology like moderate to severe aortic stenosis, mitral stenosis and primary mitral regurgitation
    • Planned organ transplantation (or in listing for transplantation), planned cardiac or other major surgery (including ventricular assist device implantation)

Other illness

  • Patients with history of suspected or proven angioedema or unable to tolerate ACEIs, ARBs or ARNI (e.g., due to cough, hypotension, renal dysfunction, hyperkalemia)
  • Patients requiring continuous intravenous inotropic therapy or with indication of advanced support intervention for HF:
    • already on list for a heart transplantation
    • with current indication of left ventricular assist device, or cardiac resynchronization therapy (CRT)
  • Severe gastrointestinal form of chronic Chagas' disease (demonstrated megaesophagus and/or important megacolon, e.g.: with compromised oral intake or surgical indication).
  • Clinical conditions or systemic diseases limiting proper patient participation
  • History of malignancy of any organ system within the past 5 years.
  • Current confirmed COVID19 infection
  • Past COVID19 infection with persistent symptom burden suspected due to COVID19 (persistent symptoms may include, but are not limited to, continued cough, breathing difficulty, muscle/joint aches, and gastrointestinal symptoms from the time of COVID19 infection onward)

Lab values

  • Serum potassium \> 5.2 mmol/L
  • Estimated glomerular filtration rate (eGFR) \< 30 mL/min/1.73 m2 of body surface area

Other

  • Use of sacubitril/valsartan in the past 3 months
  • Systemic systolic blood pressure lower than 95 mmHg or symptomatic hypotension
  • Pregnant or nursing women or women of child-bearing potential unless they are using highly effective methods of contraception

Who the study is looking for

  • Male or female ≥ 18 years of age
  • Diagnosis of NYHA Class II-IV HFrEF established by:
    • LVEF ≤ 40% within 12 months prior to Visit 1 made by any local measurement using echocardiography, multiple gated acquisition scan (MUGA), computerized tomography (CT) scanning, magnetic resonance imaging (MRI), or ventricular angiography, provided no subsequent measurement above 40% AND
    • NT-proBNP ≥ 600 pg/mL (or BNP ≥ 150 pg/mL) at Visit 1 OR
    • NT-proBNP ≥ 400 pg/mL (or BNP ≥ 100 pg/mL) at Visit 1 and a hospitalization for HF within the last 12 months
  • Chagas' disease diagnosis confirmed by at least two different serological tests for anti-Trypanosoma cruzi based on different principles or with different antigenic preparations, such as: enzyme-linked immunosorbent assay \[ELISA\], indirect immunofluorescence \[IFI\], indirect hemagglutination \[IHA\], western blot (WB), chemiluminescent immunoassay (CLIA). If documented history is not available, the tests may be performed during the screening

Age in the registry: 18 years to 100 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (54)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Novartis Investigative Site
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Buenos AiresArgentinaUnknown status
Novartis Investigative Site
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CABAArgentinaUnknown status
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CórdobaArgentinaUnknown status
Novartis Investigative Site
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CorrientesArgentinaUnknown status
Novartis Investigative Site
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FormosaArgentinaUnknown status
Novartis Investigative Site
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MendozaArgentinaUnknown status
Novartis Investigative Site
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Ramos MejíaArgentinaUnknown status
Novartis Investigative Site
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RosarioArgentinaUnknown status
Novartis Investigative Site
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SaltaArgentinaUnknown status
Novartis Investigative Site
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San MartínArgentinaUnknown status
Novartis Investigative Site
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San Miguel de TucumánArgentinaUnknown status
Novartis Investigative Site
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San Miguel TucumanArgentinaUnknown status
Novartis Investigative Site
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Santa FeArgentinaUnknown status
Novartis Investigative Site
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Santiago del EsteroArgentinaUnknown status
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TemperleyArgentinaUnknown status
Novartis Investigative Site
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Villa MaríaArgentinaUnknown status
Novartis Investigative Site
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BelémBrazilUnknown status
Novartis Investigative Site
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Belo HorizonteBrazilUnknown status
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BotucatuBrazilUnknown status
Novartis Investigative Site
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Bragança PaulistaBrazilUnknown status
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BrasilaBrazilUnknown status
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BrasíliaBrazilUnknown status
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CampinasBrazilUnknown status
Novartis Investigative Site
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FortalezaBrazilUnknown status
Novartis Investigative Site
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GoiâniaBrazilUnknown status
Novartis Investigative Site
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IjuíBrazilUnknown status
Novartis Investigative Site
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IndaiatubaBrazilUnknown status
Novartis Investigative Site
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LondrinaBrazilUnknown status
Novartis Investigative Site
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MaríliaBrazilUnknown status
Novartis Investigative Site
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Montes ClarosBrazilUnknown status
Novartis Investigative Site
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PassosBrazilUnknown status
Novartis Investigative Site
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RecifeBrazilUnknown status
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Ribeirão PretoBrazilUnknown status
Novartis Investigative Site
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Rio de JaneiroBrazilUnknown status
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SalvadorBrazilUnknown status
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Santo AndréBrazilUnknown status
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Sao Jose Rio PretoBrazilUnknown status
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São LuísBrazilUnknown status
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São PauloBrazilUnknown status
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TatuíBrazilUnknown status
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TeresinaBrazilUnknown status
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UberabaBrazilUnknown status
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UberlândiaBrazilUnknown status
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VotuporangaBrazilUnknown status
Novartis Investigative Site
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BogotaColombiaUnknown status
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Bogota DCColombiaUnknown status
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FloridablancaColombiaUnknown status
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Florida BlancaColombiaUnknown status
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San GilColombiaUnknown status
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Santa MartaColombiaUnknown status
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Ciudad deMexicoUnknown status
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MéridaMexicoUnknown status
Novartis Investigative Site
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Oaxaca CityMexicoUnknown status
Novartis Investigative Site
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XalapaMexicoUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.