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Sleep Apnea-hypopnea Syndrome (SAHS) and Ventricular Arrhythmias (SAHS-ICD)

Primary Purpose

Sleep Apnea, Ventricular Arrythmias, Systolic Left Ventricle Dysfunction

Status
Completed
Phase
Phase 4
Locations
Spain
Study Type
Interventional
Intervention
Nasal continuous positive airway pressure
Sponsored by
Hospital Universitario La Paz
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sleep Apnea focused on measuring Sleep apnea, CPAP, Ventricular arrhythmias, Defibrillator therapies

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Previous diagnostic of ischaemic heart disease of dilated myocardiopathy
  • Ejection fraction of left ventricle < 40%
  • Patients with implantable cardioverter-defibrillator

Exclusion Criteria:

  • Diurnal hypersomnolence with EES > 16
  • Morbid obesity (BMI > 35 Kg/m2).
  • Moderate-severe chronic obstructive pulmonary disease (FEV1/FVC < 70 % and FEV1 < 80 % of reference).
  • Known thyroid disease.
  • Previous treatment with CPAP.

Sites / Locations

  • Hospital Universitario La Paz
  • Hospital Universitario Virgen de la Macarena
  • Hospital Virgen de la Salud

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

CPAP

Conventional

Arm Description

Continuous positive airway pressure

Hygienic-dietetic recommendations

Outcomes

Primary Outcome Measures

Number of appropriate defibrillator therapies

Secondary Outcome Measures

AHI, incidence of premature ventricular beats and non-sustained ventricular tachycardia. Plasmatic levels of C-reactive protein, homocystein, pro-BNP, sTNFαR-I, IL-1b, IL-2, IL-6, IL-8, IL-8 and 8-isoprostane

Full Information

First Posted
October 2, 2008
Last Updated
April 1, 2013
Sponsor
Hospital Universitario La Paz
Collaborators
Hospital Virgen de la Salud, Hospital Universitario Virgen Macarena
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1. Study Identification

Unique Protocol Identification Number
NCT00765713
Brief Title
Sleep Apnea-hypopnea Syndrome (SAHS) and Ventricular Arrhythmias
Acronym
SAHS-ICD
Official Title
Sleep Apnea-hypopnea Syndrome and Ventricular Arrhythmias in Patients With Systolic Ventricular Dysfunction and Implantable Cardioverter-defibrillator. Incidence and Effect of CPAP Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
September 2008
Overall Recruitment Status
Completed
Study Start Date
October 2008 (undefined)
Primary Completion Date
October 2012 (Actual)
Study Completion Date
January 2013 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Hospital Universitario La Paz
Collaborators
Hospital Virgen de la Salud, Hospital Universitario Virgen Macarena

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Hypothesis: The CPAP treatment diminishes the effect of ventricular arrhythmias in patients with ischemic heart disease or dilated myocardiopathy, systolic ventricular disfunction and sleep apnea-hypopnea syndrome (SAHS)Objectives: To analyze the incidence of ventricular arrhythmias (premature ventricular beat, non-sustained ventricular tachycardia and sustained ventricular tachycardia) and appropriate defibrillator therapies in patients with ischemic heart disease or dilated myocardiopathy, moderate-severe left ventricular dysfunction,with an implantable cardioverter-defibrillator (ICD) and sleep apnea. To study the effect of CPAP on the cardiac arrhythmias and on the number of appropriate defibrillator therapies. Design: Parallel, randomized and single-blinded multicentric study to compare CPAP vs. hygienic-dietetic recommendations. Patients with SAHS (AHI≥15) and systolic left ventricle dysfunction patients with an ICD. Duration: 24 months.
Detailed Description
Secondary objectives: To compare the prevalence of SAHS in patients with ischemic heart disease or dilated myocardiopathy and moderate-severe left ventricle dysfunction with ICD with that of the general population. To study the incidence of supraventricular arrhythmias (atrial fibrillation, atrial flutter or supraventricular tachycardia) and inappropriate defibrillator therapies in these patients. To value the effect of the treatment with CPAP on the above mentioned arrhythmias. To relate the effect of ventricular and supraventricular arrhythmias with sleep parameters, cardiovascular biomarkers, inflammation and oxidative stress. To evaluate the long-term effect of the CPAP on systemic biomarkers in patients with ischemic heart disease or dilated myocardiopathy and moderate-severe left ventricle dysfunction. To evaluate the long-term effect of CPAP on the quality of life in these patients. Sample size: 224 patients with ischemic heart disease or dilated myocardiopathy and moderate-severe left ventricle dysfunction with ICD will be included to randomize 19 SAHS subjects for arm.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Apnea, Ventricular Arrythmias, Systolic Left Ventricle Dysfunction
Keywords
Sleep apnea, CPAP, Ventricular arrhythmias, Defibrillator therapies

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
224 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CPAP
Arm Type
Experimental
Arm Description
Continuous positive airway pressure
Arm Title
Conventional
Arm Type
No Intervention
Arm Description
Hygienic-dietetic recommendations
Intervention Type
Device
Intervention Name(s)
Nasal continuous positive airway pressure
Intervention Description
Nocturnal
Primary Outcome Measure Information:
Title
Number of appropriate defibrillator therapies
Time Frame
24 months
Secondary Outcome Measure Information:
Title
AHI, incidence of premature ventricular beats and non-sustained ventricular tachycardia. Plasmatic levels of C-reactive protein, homocystein, pro-BNP, sTNFαR-I, IL-1b, IL-2, IL-6, IL-8, IL-8 and 8-isoprostane
Time Frame
24 moths

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Previous diagnostic of ischaemic heart disease of dilated myocardiopathy Ejection fraction of left ventricle < 40% Patients with implantable cardioverter-defibrillator Exclusion Criteria: Diurnal hypersomnolence with EES > 16 Morbid obesity (BMI > 35 Kg/m2). Moderate-severe chronic obstructive pulmonary disease (FEV1/FVC < 70 % and FEV1 < 80 % of reference). Known thyroid disease. Previous treatment with CPAP.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francisco Garcia-Rio, PhD
Organizational Affiliation
Hospital Universitario La Paz
Official's Role
Study Director
Facility Information:
Facility Name
Hospital Universitario La Paz
City
Madrid
ZIP/Postal Code
28046
Country
Spain
Facility Name
Hospital Universitario Virgen de la Macarena
City
Sevilla
Country
Spain
Facility Name
Hospital Virgen de la Salud
City
Toledo
Country
Spain

12. IPD Sharing Statement

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Sleep Apnea-hypopnea Syndrome (SAHS) and Ventricular Arrhythmias

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