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
- Diseases
- Heart failure
- 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
Sites (54)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Novartis Investigative Site Coordinator of this site? Confirm its status | Buenos Aires | Argentina | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | CABA | Argentina | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Córdoba | Argentina | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Corrientes | Argentina | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Formosa | Argentina | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Mendoza | Argentina | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Ramos Mejía | Argentina | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Rosario | Argentina | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Salta | Argentina | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | San Martín | Argentina | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | San Miguel de Tucumán | Argentina | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | San Miguel Tucuman | Argentina | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Santa Fe | Argentina | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Santiago del Estero | Argentina | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Temperley | Argentina | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Villa María | Argentina | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Belém | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Belo Horizonte | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Botucatu | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Bragança Paulista | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Brasila | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Brasília | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Campinas | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Fortaleza | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Goiânia | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Ijuí | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Indaiatuba | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Londrina | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Marília | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Montes Claros | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Passos | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Recife | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Ribeirão Preto | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Rio de Janeiro | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Salvador | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Santo André | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Sao Jose Rio Preto | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | São Luís | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | São Paulo | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Tatuí | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Teresina | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Uberaba | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Uberlândia | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Votuporanga | Brazil | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Bogota | Colombia | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Bogota DC | Colombia | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Floridablanca | Colombia | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Florida Blanca | Colombia | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | San Gil | Colombia | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Santa Marta | Colombia | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Ciudad de | Mexico | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Mérida | Mexico | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Oaxaca City | Mexico | Unknown status |
| Novartis Investigative Site Coordinator of this site? Confirm its status | Xalapa | Mexico | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.