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TerminatedNCT00511888Updated Oct 17, 2008

Nebivolol Versus Carvedilol in Patients With Heart Failure

An observational study in Chronic Heart Failure and Hypertension, sponsored by IRCCS San Raffaele. Terminated at 1 site in Italy. Open to participants aged 53 Years to 76 Years. Per ClinicalTrials.gov, last updated 2008-10-17.

Sponsored by IRCCS San Raffaele · Observational

Why this study was terminated
is finish
Study type
Observational
Time perspective
Prospective
Enrollment
160
Ages
53 Years to 76 Years
Sex
All
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Study summary

BACKGROUND Beta-blockers improve left ventricular (LV) systolic function and prognosis in patients with chronic heart failure. Both carvedilol and nebivolol have hemodynamic and clinical benefits in chronic heart failure (CHF), but it is unknown whether their pleiotropic properties may play a role in different subgroups of patients with CHF.

OBJECTIVE: To compare the effects of nebivolol and carvedilol on LV function and clinical outcome in patients with chronic heart failure and reduced LV systolic function.

METHODS: 160 hypertensive CHF patients, LV ejection fraction (EF) 40% and in New York Heart Association (NYHA) functional class II or III were randomly assigned to receive carvedilol or nebivolol therapy for 24 months. At baseline and after 24 months of treatment, all patients underwent clinical evaluation: echocardiogram and 6-minute walking test.

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Conditions studied

  • Chronic Heart Failure
  • Hypertension

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Keywords

  • chronic heart failure
  • hypertension
  • beta blockers
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In context

Hypertension

6,834 studies on the registry are indexed under Hypertension; 971 are open to participants now.

This study's enrollment of 160 is below the median of 210 across 1,392 observational studies indexed under Hypertension.

Browse Hypertension studies →

Lead sponsor

IRCCS San Raffaele is the lead sponsor of 451 studies on the registry; 235 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
53 Years to 76 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • left ventricular ejection fraction (LVEF) \< 40%;
  • symptomatic heart failure with functional New York Heart Association (NYHA) class II or III;
  • arterial hypertension with systolic blood pressure >140 mmHg and diastolic blood pressure >85 mmHg;
  • clinical stability without hospital admission for heart failure in the previous 3 months.

Exclusion criteria

Exclusion Criteria:

  • history of asthma or severe chronic obstructive pulmonary disease;
  • severe liver or kidney diseases;
  • second-degree or third degree heart block without a permanent pacemaker,
  • sick sinus syndrome, heart rate \<60 beat/min, systolic blood pressure \<90 mmHg.
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Study design

Time perspective
Prospective
Enrollment
160 participants (actual)
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Study locations

1 site
  • IRCCS San Raffaele
    Rome, rome 00163, Italy
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 17, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00511888
Lead sponsor
IRCCS San Raffaele
First posted
Aug 6, 2007
Start date
Jan 2004
Completion
Jun 2007
Last update
Oct 17, 2008

Study contacts

giuseppe rosano, md
study director · IRCCS san Raffaele Cardiovascular Research Unit

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Aug 2007. You cannot join it, but the record below documents what was studied.

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