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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00517725
Other study ID # R76-CCM S78/407
Secondary ID
Status Completed
Phase Phase 4
First received August 16, 2007
Last updated September 15, 2010
Start date July 2007
Est. completion date May 2010

Study information

Verified date September 2010
Source Centro Cardiologico Monzino
Contact n/a
Is FDA regulated No
Health authority Italy: Ministry of Health
Study type Interventional

Clinical Trial Summary

The investigators test the hypothesis that different beta-blockers had a different influence on chemoreceptor response and lung diffusion capacity.

Both could influence exercise capacity in normoxic as well as hypoxic conditions.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date May 2010
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Chronic heart failure patients in stable clinical condition

Exclusion Criteria:

- No comorbidity

- NYHA class IV

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
carvedilol

bisoprolol

Nebivolol


Locations

Country Name City State
Italy Centro Cardiologico Monzino, University of Milan Milan

Sponsors (1)

Lead Sponsor Collaborator
Centro Cardiologico Monzino

Country where clinical trial is conducted

Italy, 

References & Publications (1)

Agostoni P, Bussotti M, Cattadori G, Margutti E, Contini M, Muratori M, Marenzi G, Fiorentini C. Gas diffusion and alveolar-capillary unit in chronic heart failure. Eur Heart J. 2006 Nov;27(21):2538-43. Epub 2006 Oct 6. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary exercise capacity two months
Secondary lung diffusion two months
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