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Trial information

A Study of the Effect of CPAP in Patients With Diastolic Heart Failure and Sleep-Related Breathing Disorder.

Status: Recruiting

Protocol number: RD000000388

Company division: Diagnostic

Official Scientific Title: Evaluation of the efficacy of treatment with CPAP (continuous postive airway pressure) in patients with diastolic HF (HF with systolic function preserved) and sleep-related breathing disorder.

Brief summary: This study will evaluate the efficacy of treatment with continuous postive airway pressure (as assessed by measurement of NT-proBNP and a number of echocardiographic variables) in patients with diastolic heart failure and sleep-related breathing disorders. The effect of reversing signs of diastolic dysfunction on long term prognosis in these patients will be evaluated.

Condition: Sleep Apnea Syndromes

Intervention type: Diagnostic Test

Intervention name: ELECSYS®proBNP

Inclusion criteria:

  • >=1 documented episode of heart failure;
  • clinically stable;
  • no change of treatment in the month prior to inclusion in the study;
  • presence of >=2 abnormal diastolic function indices.

Exclusion criteria:

  • base rhythm different from normal sinus rhythm;
  • severe lung disease;
  • significant primary heart disease;
  • unstable angina pectoris, acute myocardial infarction or heart surgery in 3 months prior to inclusion in study.

Gender: Males or Females

Age limits: Min: 40 Years Max: 80 Years

Accepts healthy volunteers: No

Anticipated start date: February, 2006

Trial registration date: 12/06/2006

Date last updated: 9/29/2008


Link to trial result

This trial is being conducted at the following locations:

Portugal

  • Coimbra
  • Porto

Spain

  • Madrid
  • Santander
  • Santiago
  • Valladolid
  • Vitoria

To contact Roche for more information on this trial please complete the email form below. Treatment decisions and/or suitability for a specific trial are decisions only your healthcare provider can make. If you are patient interested in any of the studies, please have your healthcare provider contact us via this website, and they will be provided with the relevant clinical trial information.

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