Acute Heart FailureREPORT-HFNCT02595814
Global Non-interventional Heart Failure Disease Registry
An observational study of Acute Heart Failure, run by Novartis Pharmaceuticals at 346 sites in 44 countries.
Trial summary
The clinical characteristics, initial presentation, management, and outcomes of patients hospitalized with new-onset (first diagnosis) heart failure (HF) or decompensation of chronic HF are poorly understood worldwide. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Acute Heart Failure
- How many people
- 18,805 participants
- Where
- 346 sitesin 44 countries
- Study dates
- 23 Jul 2014to 31 Mar 2018
- How long will I take part?
- 3 Years
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Enrollment of adult patients hospitalized with a primary diagnosis of acute Heart Failure (HF), i.e. new-onset (first diagnosis) HF or decompensation of chronic HF
Who may be able to join
- Patients at least 18 years old, or older for those countries where the adult age is above 18 years of age, hospitalized with a primary diagnosis of acute heart failure.
Who cannot join
- 1-Concomitant participation in any/a clinical trial with any investigational treatment (for any sponsor).
- 2. Use of investigational drugs within 5 half-lives of enrollment, or until the expected pharmacodynamic effect has returned to baseline, whichever is longer.
Trial locations and contacts
346 sites in 44 countries.
346 sites in 44 countries
China29 sites
Novartis Investigative Site
Baotou, Inner Mongolia, 014040
Novartis Investigative Site
Beijing, Beijing Municipality, 100044
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Beijing, Beijing Municipality, 100191
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Beijing, 100022
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Beijing, 100029
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Beijing, 100034
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Beijing, 100053
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Beijing
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Changchun, Jilin, 130021
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Changsha, Hunan, 410005
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Changsha, Hunan, 410011
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Dalian, Liaoning, 116011
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Fuzhou, Fujian
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Guangzhou, Guangdong, 510080
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Guangzhou, 510260
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Hangzhou, 310006
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Jinan, 250012
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Luoyang, 471000
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Shanghai, 200080
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Shijiazhuang, Hebei, 050000
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Taiyuan
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Ürümqi, 830000
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Ürümqi, 830054
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Wuhan, Hubei, 430074
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Wuhan, 430022
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Xiamen, 361004
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Yangzhou, 225001
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Zhengzhou, 450003
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Zhengzhou
India25 sites
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Ahmedabad, Gujarat, 380 060
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Amritsar, Punjab, 143004
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Bangalore, Karnataka, 560 069
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Bangalore, Karnataka, 560099
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Chennai, Tamil Nadu, 600037
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Gurgaon, Haryana, 122001
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Hyderabad, Telangana, 500034
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Hyderabad, Telangana, 500082
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India, 560040
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Kolkata, West Bengal, 700 107
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Kolkata, West Bengal, 700099
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Ludhiana, Punjab, 141001
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Ludhiana, Punjab, 141008
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Manipal, Karnataka, 576104
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Mumbai, 400053
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Nagpur, Maharashtra, 440008
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New Delhi, National Capital Territory of Delhi, 110 060
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New Delhi, National Capital Territory of Delhi, 110017
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New Delhi, National Capital Territory of Delhi, 110070
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New Delhi, 110002
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New Delhi, 110025
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Panjim, Goa, 403001
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Pune, Maharashtra, 411 011
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Pune, Maharashtra, 411011
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Vadodara, Gujarat, 390022
Russia18 sites
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Kazan', 420033
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Kemerovo, 654005
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Krasnodar, 350086
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Moscow, 117292
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Moscow, 127473
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Novosibirsk, 630091
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Ryazan, 390026
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S-Petersburg, 194354
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Saint Petersburg, 191015
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Saint Petersburg, 194044
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Saint Petersburg, 197341
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Saratov, 410004
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Saratov, 410017
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Stavropol, 355030
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Tyumen, 625023
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Ulyanovsk, 432057
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Vladivostok, 690002
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Volgograd, 400026
United States15 sites
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Chicago, Illinois, 60611
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Cincinnati, Ohio, 45267
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Dallas, Texas, 75390
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Detroit, Michigan, 48201
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Detroit, Michigan, 48202
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Indianapolis, Indiana, 46202
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Jackson, Mississippi, 39216
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Kansas City, Kansas, 66160
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Nashville, Tennessee, 37203
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New Orleans, Louisiana, 70112
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New Orleans, Louisiana, 70121
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New York, New York, 10029
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San Diego, California, 92103
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San Francisco, California, 94143-0780
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Stony Brook, New York, 11794
Argentina15 sites
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Buenos Aires, Buenos Aires F.D., 1118
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Buenos Aires, C1094AAD
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Buenos Aires, C1426EOB
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Buenos Aires
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CABA, Buenos Aires, C1181ACH
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CABA, Buenos Aires, C1210AAP
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Córdoba, X5000JHQ
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Córdoba, X5000
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Coronel Suarez, Buenos Aires F.D., 7540
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Corrientes, W3400AFT
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Mendoza, M5500AAJ
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Resistencia, Chaco Province, H3500CDM
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Rosario, Santa Fe Province, 2000
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Rosario, Santa Fe Province, S2000DSV
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Salta, 4000
Germany13 sites
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Berlin, 13353
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Bonn, 53105
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Essen, 45356
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Freiburg im Breisgau, 79106
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Göttingen, 37075
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Halle, 06120
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Hanover, 30625
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Heidelberg, 69120
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Homburg, 66421
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Lübeck, 23538
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Ludwigshafen, 67063
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Nuremberg, 90471
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Würzburg, 97078
Spain13 sites
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Alicante, Valencia, 03010
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Barakaldo, Basque Country, 48903
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Barcelona, Catalonia, 08035
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Barcelona, Catalonia, 08036
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Barcelona, 08041
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Córdoba
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Las Palmas de Gran Canaria, Las Palmas de G.C, 35020
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León, 24080
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Majadahonda, Madrid, 28222
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Mallorca, Balearic Islands, 07198
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Mérida, Extremadura, 06800
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Murcia, 30008
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Tarragona, Catalonia, 43005
Greece11 sites
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Athens, GR, 115 25
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Athens, GR, 115 27
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Athens, GR, 11527
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Athens, 11526
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Athens, 54642
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Athens, GR 115 22
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Glyfada, 16675
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Ioannina, 45100
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Piraeus, 18454
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Thessaloniki, GR, 570 10
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Thessaloniki, 54642
South Korea11 sites
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Busan, 612-896
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Cheongju-si, North Chungcheong, 28644
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Daejeon, Korea, 301-721
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Gyeonggi-do, Bucheon-si, 422-711
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Incheon, 403-720
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Pusan, 614-735
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Seoul, 07061
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Seoul, 136-705
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Suwon, 16247
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Taegu, 700 -721
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Wŏnju, Gangwon-do, 220-701
Brazil10 sites
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Belo Horizonte, Minas Gerais, 30130-100
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Campinas, São Paulo, 13060-904
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Curitiba, Paraná, 80010-030
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Curitiba
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Fortaleza, Ceará, 60864-190
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Recife
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Rio de Janeiro, Rio de Janeiro, 22280-020
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Rio de Janeiro
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Sao Jose Do Rico Preto
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Tatuí, São Paulo, 18270-170
Turkey (Türkiye)10 sites
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Ankara, 06100
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Ankara, 06590
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Bursa, 16059
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Bursa
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Diskapi / Ankara, 06110
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Haydarpasa/Istanbul, 34668
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Istanbul, 34093
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Meselik / Eskisehir, 26480
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Pendik / Istanbul, Turkey, 34899
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Sivas, 58140
United Kingdom10 sites
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Bradford, West Yorkshire, BD9 6RJ
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Chesterfield, Yorkshire, S44 5BL
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Chesterfield, BS1 3NU
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Edgbaston, Birmingham, B15 2WB
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Herts, Yorkshire, SG1 4AB
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Stockton-on-Tees, Cleveland, TS19 8PE
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Telford, TF1 6TF
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Uxbridge, UB8 3NN
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Wakefield, WF1 4DG
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York, YO31 8HE
Colombia9 sites
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Armenia
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Barranquilla, Atlántico
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Bogotá, Cundinamarca, 110111
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Bogotá, 00000
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Bogotá
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Bucaramanga, Santander Department
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Cali
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Medellín, Antioquia, 0050010
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Medellín, Antioquia
Indonesia9 sites
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Bandung, West Java, 40161
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Bekasi, West Java, 17144
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East Jakarta, DKI Jakarta, 13630
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Medan, North Sumatera, 20136
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Padang, West Sumatra, 25127
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South Jakarta, DKI Jakarta, 12430
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Surabaya, East Java, 60286
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Tangerang, Banten, 15111
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West Jakarta, DKI Jakarta, 11420
Mexico9 sites
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Aguascalientes, 20230
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Culiacán, Sinaloa SN, 80230
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Mexico City, Mexico City, 03100
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Mexico City, Mexico City, 06090
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Mexico City, Mexico City, 14080
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San Luis Potosí City, 78213
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San Luis Potosí City, 78240
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Xalapa, 91020
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Xalapa, 91193
Romania8 sites
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Bucharest, 022322
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Bucharest, 030 171
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Buzău, 120140
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Cluj-Napoca, Napoca, 400006
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Cluj-Napoca, 400006
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Focşani, 620034
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Lasi, 700075
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Timișoara, 300054
Japan7 sites
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Chiyoda-ku, Tokyo, 101-8643
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Hirakata, Osaka, 573-0153
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Kita-ku, Okayama-ken, 7000084
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Kitakyushu, Fukuoka, 802-8555
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Kure, Hiroshima, 737-0023
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Nagasaki, 850-8555
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Sakaidechō, Kagawa-ken, 762-0007
Philippines7 sites
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Angeles City, Pampanga, 2009
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Baguio City, Baguio, 2600
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Cagayan de Oro City, Cagayan Valley, 9000
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Cebu City, Cebu, 6000
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Davao City, Davao Region, 8000
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Manila, National Capital Region, 1000
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Quezon City, Manila, 1100
Thailand7 sites
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Bangkok, 10310
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Bangkok, 10400
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Chiang Mai, 50200
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Khon Kaen, THA, 40002
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Muang, Muang, 65000
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Muang, Thailand, 12120
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Muang, Thailand, 30000
Bulgaria6 sites
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Pleven, 5800
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Plovdiv, 4002
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Sofia, 1202
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Sofia, 1527
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Sofia, 1606
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Varna, 9010
Lebanon6 sites
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Beirut, 1107 2020
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Beirut, 6301
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Beirut
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Byblos
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El Chouf, LBN
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Saida, 652
Netherlands6 sites
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Amsterdam, 1034CS
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Groningen, 9713 GZ
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Leiderdorp, NL-2353 GA
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Sneek, 8601ZK
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Venlo, 5912 BL
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Zwolle, 8025 AB
Sweden6 sites
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Gothenburg, 416 85
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Helsingborg, 252 20
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Karlshamn, 37480
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Linköping, 581 85
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Malmö, 205 20
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Trollhättan, 46173
Taiwan6 sites
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Linkou District, 33305
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Taichung, 40705
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Tainan, 70421
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Taipei, 10002
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Taipei, 110
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Taipei, 11217
Austria5 sites
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Eisenstadt, 7000
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Linz, 4021
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Mödling, A-2340
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Vienna, A-1160
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Vienna, A-1220
Canada5 sites
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Edmonton, Alberta, T6G 2B7
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Halifax, Nova Scotia, B3H 3A7
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Ottawa, Ontario, K1Y 4W7
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Sainte-Foy, Quebec, G1V 4G5
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Vancouver, British Columbia, V6Z 1Y6
Egypt5 sites
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Alexandria, 21411
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Cairo, 11566
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Cairo
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El Menia, Upper Egypt
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Suez Canal Region, 41111
Israel5 sites
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Jerusalem, 91031
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Jerusalem, 91240
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Kfar Saba, 4428164
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Nazareth, 16100
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Sefad, 13100
Jordan5 sites
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Amman, 11121
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Amman, 11196
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Amman, 11942
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Amman
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Irbid, 22110
Malaysia5 sites
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Alor Star, Kedah, 05460
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Johor Bahru, 80100
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Kota Bharu, Kelantan, 16150
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Kuala Lumpur, 50586
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Pulau Pinang, Pulau Pinang, 10990
Saudi Arabia5 sites
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Al Ahsa
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Dammam, 15215
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Dammam, 31463
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Khamis Mushait, 62413
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Riyadh, 3643
South Africa5 sites
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Bloemfontein, 9301
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Cape Town, 7405
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Cape Town, 7505
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Durban, KwaZulu-Natal, 4052
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Rivonia, 2128
Tunisia5 sites
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Monastir, 5000
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Sousse, 4011
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Tunis, 1006
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Tunis, 1007
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Tunis, 1008
Algeria4 sites
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Algiers, 16000
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Algiers, 16040
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Algiers, 16206
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Oran, 31000
Australia4 sites
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Auchenflower, Queensland, 4066
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Bedford Park, SA 5042
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Gosford, New South Wales, 2250
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Greenslopes, Queensland, 4120
Chile4 sites
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Concepción
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San Miguel, Santiago Metropolitan, 8900000
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Santiago, Piso 1
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Santiago
Ecuador4 sites
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Guayaquil, Guayas
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Guayaquil
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Portoviejo
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Quito, Pichincha, 1701
United Arab Emirates4 sites
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Abu Dhabi, 51900
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Al Ain City
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Dubai, 7272
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Dubai
Morocco3 sites
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Casablanca
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Marrakesh, 40 000
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Rabat, 10 000
Norway3 sites
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Hønefoss, 3501
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Oslo, 370
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Skien, NO-3710
Switzerland3 sites
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Basel, 4031
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Bruderholz, 4101
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Zurich, 8032
Guatemala2 sites
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Guatemala City, 01011
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Guatemala City
Panama2 sites
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Panama City
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San Jose de David, Provincia de Panamá
Vietnam2 sites
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Ho Chi Minh City, District 7
Novartis Investigative Site
Ho Chi Minh City
About this study
Official title: International Registry to Assess mEdical Practice With lOngitudinal obseRvation for Treatment of Heart Failure
The clinical characteristics, initial presentation, management, and outcomes of patients hospitalized with new-onset (first diagnosis) heart failure (HF) or decompensation of chronic HF are poorly understood worldwide. REPORT-HF is a global, prospective, and observational HF disease registry designed to characterize patient trajectories longitudinally during and following an index hospitalization for acute HF.
- Conditions
- Acute Heart Failure
- Keywords
- Registry, Heart failure, Hospitalized, Global, Morbidity, Mortality, Quality of life, AHF
- Medical subject headings
- Heart Failure
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of patients with different characteristics of heart faliure (HF) at hospitalization
Measured: From admission to discharge of the patient's index hospitalization (minimum 24 hours)
Percentage of patients who die during the index hospitalization
Measured: From admission to discharge of the patient's index hospitalization (minimum 24 hours)
Percentage of patients who die during the follow-up period post-discharge
Measured: up to 3 years
Percentage of patients who are re-hospitalized by primary re-hospitalization reason (Cardiovascular and non-Cardiovascular)
Measured: up to 3 years
Number of patients with different characteristics of post-discharge patient management
Measured: up to 3 years
Healthcare Resource Utilization assessed by number of patients with re-hospitalizations
Measured: up to 3 years
Secondary outcomes (3)
Health-related Quality of life (HRQoL) based on patient reported data as measured by EQ-5D and the Kansas City Cardiomyopathy Questionnaire (KCCQ) questionnaires
Measured: up to 3 years
Caregiver burden based on Caregiver Burden Questionnaire -Heart Failure (CBQ-HF) and Work Productivity and Activity Impairment (WPAI) questionnaires
Measured: up to 3 years
Correlation ratio between practice patterns and outcomes
Measured: up to 3 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Nov 2015 (estimated)
- Study start23 Jul 2014
- Primary completion31 Mar 2018
- Study completion31 Mar 2018
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (4)Papers the sponsor has linked to this study.
- Other trials for Acute Heart FailureStudies of the same condition, open and under way.
- More trials run by Novartis PharmaceuticalsThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Prospective
- Enrolment
- 18,805 participants (actual)
- Target duration
- 3 Years
Sponsor and investigators
- Lead sponsor
- Novartis Pharmaceuticals
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02595814
- Sponsor's protocol ID
- CRPORTHF
- Acronym
- REPORT-HF
- Status last verified
- Nov 2018
- First submitted
- 13 Oct 2015
- Last updated
- 14 Nov 2018
- Results posted
- No
- Data monitoring committee
- No
Publications
Filippatos G, Khan SS, Ambrosy AP, Cleland JG, Collins SP, Lam CS, Angermann CE, Ertl G, Dahlstrom U, Hu D, Dickstein K, Perrone SV, Ghadanfar M, Bermann G, Noe A, Schweizer A, Maier T, Gheorghiade M. International REgistry to assess medical Practice with lOngitudinal obseRvation for Treatment of Heart Failure (REPORT-HF): rationale for and design of a global registry. Eur J Heart Fail. 2015 May;17(5):527-33. doi: 10.1002/ejhf.262. Epub 2015 Mar 10.
PubMed 25754836Tay WT, Teng TK, Ouwerkerk W, Cleland JGF, Collins SP, Angermann CE, Dickstein K, Dahlstrom U, Schweizer A, Obergfell A, Yiu KH, Ghadanfar M, Hassanein M, Ren QW, Gu WL, Ertl G, Perrone SV, Filippatos G, Lam CSP, Tromp J. Global patterns of polypharmacy after acute heart failure hospitalization: Prevalence and outcomes from the REPORT-HF registry. Eur J Heart Fail. 2025 Dec;27(12):2705-2715. doi: 10.1002/ejhf.70056. Epub 2025 Oct 1.
PubMed 41031485Chyou JY, Tay WT, Tromp J, Ouwerkerk W, Yiu KH, Cleland JGF, Collins SP, Angermann CE, Ertl G, Dahlstrom U, Dickstein K, Perrone SV, Ghadanfar M, Schweizer A, Obergfell A, Filippatos G, Lam CSP. Prognostic Implications and Global Perspectives of Atrial Fibrillation in Patients Hospitalized for Heart Failure. JACC Heart Fail. 2025 Mar;13(3):453-464. doi: 10.1016/j.jchf.2024.11.009. Epub 2025 Feb 5.
PubMed 39918534Ouwerkerk W, Tromp J, Cleland JGF, Angermann CE, Dahlstrom U, Ertl G, Hassanein M, Perrone SV, Ghadanfar M, Schweizer A, Obergfell A, Dickstein K, Filippatos G, Collins SP, Lam CSP. Association of time-to-intravenous furosemide with mortality in acute heart failure: data from REPORT-HF. Eur J Heart Fail. 2023 Jan;25(1):43-51. doi: 10.1002/ejhf.2708. Epub 2022 Nov 23.
PubMed 36196060
Study at a glance
From the registry record, last updated by the sponsor on 14 Nov 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- International Registry to Assess mEdical Practice With lOngitudinal obseRvation for Treatment of Heart Failure
- ClinicalTrials.gov ID
- NCT02595814
- Acronym / sponsor ID
- REPORT-HF / CRPORTHF
- Conditions
- Acute Heart Failure
- Keywords
- Registry, Heart failure, Hospitalized, Global, Morbidity, Mortality, Quality of life, AHF
- Study type
- Observational
- Recruitment status
- Terminated
- Enrolment
- 18,805 participants (actual)
- Lead sponsor
- Novartis PharmaceuticalsIndustry (pharma, biotech, devices)
- Study start
- 23 Jul 2014 (actual)
- Primary completion
- 31 Mar 2018 (actual)
- Study completion
- 31 Mar 2018 (actual)
- First posted
- 3 Nov 2015 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The clinical characteristics, initial presentation, management, and outcomes of patients hospitalized with new-onset (first diagnosis) heart failure (HF) or decompensation of chronic HF are poorly understood worldwide. REPORT-HF is a global, prospective, and observational HF disease registry designed to characterize patient trajectories longitudinally during and following an index hospitalization for acute HF.
Study design
- Observational model
- Other
- Time perspective
- Prospective
- Target follow-up
- 3 Years
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Enrollment of adult patients hospitalized with a primary diagnosis of acute Heart Failure (HF), i.e. new-onset (first diagnosis) HF or decompensation of chronic HF
Key inclusion criteria (1 listed)
- Patients at least 18 years old, or older for those countries where the adult age is above 18 years of age, hospitalized with a primary diagnosis of acute heart failure.
Key exclusion criteria (2 listed)
- 1-Concomitant participation in any/a clinical trial with any investigational treatment (for any sponsor).
- 2. Use of investigational drugs within 5 half-lives of enrollment, or until the expected pharmacodynamic effect has returned to baseline, whichever is longer.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Number of patients with different characteristics of heart faliure (HF) at hospitalization
Time frame: From admission to discharge of the patient's index hospitalization (minimum 24 hours)
Percentage of patients who die during the index hospitalization
Time frame: From admission to discharge of the patient's index hospitalization (minimum 24 hours)
Percentage of patients who die during the follow-up period post-discharge
Time frame: up to 3 years
Percentage of patients who are re-hospitalized by primary re-hospitalization reason (Cardiovascular and non-Cardiovascular)
Time frame: up to 3 years
Number of patients with different characteristics of post-discharge patient management
Time frame: up to 3 years
Healthcare Resource Utilization assessed by number of patients with re-hospitalizations
Time frame: up to 3 years
3 secondary outcomes
Health-related Quality of life (HRQoL) based on patient reported data as measured by EQ-5D and the Kansas City Cardiomyopathy Questionnaire (KCCQ) questionnaires
Time frame: up to 3 years
Caregiver burden based on Caregiver Burden Questionnaire -Heart Failure (CBQ-HF) and Work Productivity and Activity Impairment (WPAI) questionnaires
Time frame: up to 3 years
Correlation ratio between practice patterns and outcomes
Time frame: up to 3 years
Results and safety
The study was stopped early. Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Nov 2018.
- Background: PubMed 25754836Filippatos G, Khan SS, Ambrosy AP, Cleland JG, Collins SP, Lam CS, Angermann CE, Ertl G, Dahlstrom U, Hu D, Dickstein K, Perrone SV, Ghadanfar M, Bermann G, Noe A, Schweizer A, Maier T, Gheorghiade M. International REgistry to assess medical Practice with lOngitudinal obseRvation for Treatment of Heart Failure (REPORT-HF): rationale for and design of a global registry. Eur J Heart Fail. 2015 May;17(5):527-33. doi: 10.1002/ejhf.262. Epub 2015 Mar 10.
- Derived from this study: PubMed 41031485Tay WT, Teng TK, Ouwerkerk W, Cleland JGF, Collins SP, Angermann CE, Dickstein K, Dahlstrom U, Schweizer A, Obergfell A, Yiu KH, Ghadanfar M, Hassanein M, Ren QW, Gu WL, Ertl G, Perrone SV, Filippatos G, Lam CSP, Tromp J. Global patterns of polypharmacy after acute heart failure hospitalization: Prevalence and outcomes from the REPORT-HF registry. Eur J Heart Fail. 2025 Dec;27(12):2705-2715. doi: 10.1002/ejhf.70056. Epub 2025 Oct 1.
- Derived from this study: PubMed 39918534Chyou JY, Tay WT, Tromp J, Ouwerkerk W, Yiu KH, Cleland JGF, Collins SP, Angermann CE, Ertl G, Dahlstrom U, Dickstein K, Perrone SV, Ghadanfar M, Schweizer A, Obergfell A, Filippatos G, Lam CSP. Prognostic Implications and Global Perspectives of Atrial Fibrillation in Patients Hospitalized for Heart Failure. JACC Heart Fail. 2025 Mar;13(3):453-464. doi: 10.1016/j.jchf.2024.11.009. Epub 2025 Feb 5.
- Derived from this study: PubMed 36196060Ouwerkerk W, Tromp J, Cleland JGF, Angermann CE, Dahlstrom U, Ertl G, Hassanein M, Perrone SV, Ghadanfar M, Schweizer A, Obergfell A, Dickstein K, Filippatos G, Collins SP, Lam CSP. Association of time-to-intravenous furosemide with mortality in acute heart failure: data from REPORT-HF. Eur J Heart Fail. 2023 Jan;25(1):43-51. doi: 10.1002/ejhf.2708. Epub 2022 Nov 23.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
346 sites in 44 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Acute Heart Failure, run by Novartis Pharmaceuticals at 346 sites in 44 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 14 Nov 2018. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 346 sites in China, India, Russia, United States, Argentina and 39 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was stopped early. Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of patients with different characteristics of heart faliure (HF) at hospitalization (time frame: From admission to discharge of the patient's index hospitalization (minimum 24 hours)). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02595814, which also lists 4 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Nov 2018; AzTrials last refreshed its copy on 31 Oct 2026.