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Trial record 70 of 242 for:    furosemide

Effect of a New Formulation of Torasemide (Prolonged Release)on Myocardial Fibrosis in Patients With Heart Failure. (TORAFIC)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00409942
Recruitment Status : Completed
First Posted : December 12, 2006
Last Update Posted : July 15, 2009
Information provided by:
Ferrer Internacional S.A.

Brief Summary:

Torasemide is a loop diuretic (pyridine-sulfonylurea)with a wide experience in the treatment of oedema associated to heart failure, kidney or liver disease and either in the treatment of arterial hypertension (alone or combined with other anti-hypertensive drugs). It has been developed a new formulation of Torasemide (Torasemide prolonged release).

The aim of this trial is to study the effects of Torasemide prolonged released in comparison with furosemide, in the reduction of myocardial fibrosis in patients with chronic heart failure (Class II-IV of the New York Heart Association Classification.

Condition or disease Intervention/treatment Phase
Congestive Heart Failure Drug: Torasemide Prolonged Release Drug: Furosemide Phase 4

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 142 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Prospective, Randomised, Open, Blinded-endpoint Study of Torasemide Prolonged Release vs Furosemide to Evaluate the Efficacy on Myocardial Fibrosis in Patients With Heart Failure
Study Start Date : March 2007
Actual Primary Completion Date : June 2009
Actual Study Completion Date : June 2009

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Heart Failure

Arm Intervention/treatment
Experimental: 1
Torasemide prolonged released
Drug: Torasemide Prolonged Release
Torasemide Prolonged release 10mg/day up to 40mg/day, treatment duration:8 months
Other Name: Torasemide Prolonged release:Sutril neo

Active Comparator: 2
Drug: Furosemide
Furosemide 40mg/day up to 160mg/day, Treatment duration:8 months
Other Name: Furosemide: Seguril

Primary Outcome Measures :
  1. Myocardial fibrosis reduction:measure of Serum carboxy-terminal peptide of procollagen type 1. [ Time Frame: 8 months ]

Secondary Outcome Measures :
  1. Clinical improvement (New York Heart Association classification, signs and symptoms of heart failure) [ Time Frame: 8 months ]
  2. Cardiovascular events [ Time Frame: 8 months ]
  3. NT-proBNP (Brain Natriuretic Peptide) [ Time Frame: 8 months ]
  4. Hospitalizations, home care due to cardiovascular causes related to heart failure [ Time Frame: 8 months ]
  5. Safety and tolerability [ Time Frame: 8 months ]
  6. Quality of Life (Minnesota Test) [ Time Frame: 8 months ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Aged over 18
  • Patients with chronic heart failure class II-IV (NYHA)due to arterial hypertension
  • Patients clinically stable who required diuretic treatment
  • Patients with left ventricular hypertrophy diagnosed by echocardiogram
  • Patients without ischaemic cardiopathy or non recent disease
  • Signed Informed Consent

Exclusion Criteria:

  • Heart Failure due to aortic stenosis or hypertrophic myocardiopathy
  • Recent coronary syndrome (less than 3 months)
  • Recent myocardial infarction (less than 6 months)
  • Unstable angor pectoris
  • Severe cardiac arrhythmia
  • Pregnancy or breastfeeding
  • Aldosterone antagonists (last 6 months)
  • Current loop diuretic treatment over study doses (torasemide > 10mg/day furosemide > 40 mg/day)
  • known hypersensitivity to study drugs
  • Liver disease (SGPT or AST > twice upper normal limt)
  • Renal impairment (Serum creatinine > 2,5mg/dl)
  • Insulin-dependent diabetes
  • Patient included in another simultaneous study
  • Lactose intolerance
  • Lithium Concomitant treatment
  • Chronic treatment with NSAIDs
  • Concomitant treatment with aminoglycoside antibiotics,etacrynic acid

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00409942

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Central Hospital
Oviedo, Asturias, Spain
Canet de Mar, Primary Care Centre
Canet de Mar, Barcelona, Spain
Centelles - Primar Care Centre
Centellas, Barcelona, Spain
El Maresme - Primary Care Centre
Mataró, Barcelona, Spain
Remei, Primary care centre
Vic, Barcelona, Spain
Begonte - Primary Care Centre
Begonte, Lugo, Spain
Clinico Universitario Virgen de la Victoria
Málaga, Malaga, Spain
Donostia Hospital
Donostia, San Sebastián, Spain
Alcover - primary care centre
Alcover, Tarragona, Spain
Clinc Hospital
Barcelona, Spain
Germans Trias i Pujol Hospital
Barcelona, Spain
H. del Mar
Barcelona, Spain
Valle Hebrón Hospital
Barcelona, Spain
Reina Sofia Hospital
Córdoba, Spain
Josep Trueta Hospital
Girona, Spain
San Jorge Hospital
Huesca, Spain
Complejo Hospitalario Juan Canalejo
La Coruña, Spain
Gregorio Marañón Hospital
Madrid, Spain
Virgen de la Arrixaca
Murcia, Spain
Clinico Universitario Hospital
Salamanca, Spain
Clinico Universitario de Santiago
Santiago de Compostela, Spain
General Hospital
Valencia, Spain
Clinico Universitario
Zaragoza, Spain
Sponsors and Collaborators
Ferrer Internacional S.A.
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Study Chair: Antonio Coca, MD, PhD Hospital Clinic of Barcelona
Study Chair: Manuel Anguita, MD, PhD Hospital Reina Sofia - Córdoba
Study Chair: Eduardo De Teresa, MD, PhD Hospital Clinico - Málaga
Study Chair: Alfonso Castro Beiras, MD, PhD Hospital Juan Canalejo - Coruña
Study Director: Javier Díez Centro Investigación Médica Aplicada (CIMA) - Pamplona (Navarra)

Publications automatically indexed to this study by Identifier (NCT Number):
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Responsible Party: Savion Gropper, ferrer Identifier: NCT00409942     History of Changes
Other Study ID Numbers: N/GF-TORAFIC-06
EudraCT number 2006-001446-14
First Posted: December 12, 2006    Key Record Dates
Last Update Posted: July 15, 2009
Last Verified: June 2009
Keywords provided by Ferrer Internacional S.A.:
Chronic heart failure
Torasemide prolonged release
Myocardial fibrosis
Loop diuretics
Peptide of procollagen type 1
Additional relevant MeSH terms:
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Heart Failure
Heart Diseases
Cardiovascular Diseases
Pathologic Processes
Natriuretic Agents
Physiological Effects of Drugs
Sodium Potassium Chloride Symporter Inhibitors
Membrane Transport Modulators
Molecular Mechanisms of Pharmacological Action
Antihypertensive Agents