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Continues Positive Airway Pressure Treatment for Patients With Dilated Cardiomyopathy and Obstructive Sleep Apnea (RIDA)

Primary Purpose

Dilated Cardiomyopathy, Obstructive Sleep Apnea

Status
Unknown status
Phase
Phase 3
Locations
Sweden
Study Type
Interventional
Intervention
Continues Positive Airway Pressure (CPAP)
Sponsored by
Göteborg University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dilated Cardiomyopathy

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Patients with newly diagnosed or previously known DCM, treated and followed at cardiology outpatients clinic, stable in their symptoms and functional class at least 2 weeks after the last medicine change.

  • Consent for the study.
  • EF ≤ 45%.
  • OSA diagnosis (Apnea-Hypopnea index> = 15 in the sleep recording below).

Exclusion Criteria:

  • Patients already treated with Continues Positive Airway Pressure.
  • Patients with claustrophobia

Sites / Locations

  • Sahlgrenska University Hospital/ÖstraRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Continues Positive Airway Pressure

Consultation of conservative measures

Arm Description

Use of Continues Positive Airway Pressure (CPAP) mask every night under six months period.

Study participants with DCM and OSA (no-CPAP), participants receive consultation of conservative measures such as avoiding alcohol before bedrest, sleeping on the side...

Outcomes

Primary Outcome Measures

Change in left ventricular ejection fraction (LVEF) six months after randomization to Continues Positive Airway Pressure (CPAP) treatment or consultation of conservative measures
The primary endpoint is left ventricular ejection fraction (LVEF) measured by cardiac magnetic resonance (improvement of at least 4%) at study baseline and at 6 months after randomization to Continues Positive Airway Pressure (CPAP) or consultation of conservative measures.
Change in left ventricular ejection fraction (LVEF) six months after randomization to Continues Positive Airway Pressure (CPAP) treatment or consultation of conservative measures
The primary endpoint is left ventricular ejection fraction (LVEF) measured by echocardiography at study baseline and at 6 months after randomization to Continues Positive Airway Pressure (CPAP) or consultation of conservative measures.

Secondary Outcome Measures

Change in measurements of diastolic function after randomization to Continues Positive Airway Pressure (CPAP) or consultation of conservative measures.
Secondary outcomes include measurements of diastolic function measured by cardiac magnetic resonance (CMR) and echocardiography,
Change in measurements of cardiovascular biomarkers at
Analyzing change in cardiovascular biomarkers by analyzing blood samples
Change in quality of life questioners
Analyzing participants response to quality of life by analyzing established questioners regarding dilated cardiomyopathy (Kansas city cardiomyopathy questionnaire KCCQ).
Change in day-time sleepiness
Analyzing participants respons to established questioners regarding sleep apnea (Epworth sleepiness scale ESS) and

Full Information

First Posted
September 9, 2016
Last Updated
March 6, 2018
Sponsor
Göteborg University
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1. Study Identification

Unique Protocol Identification Number
NCT02989181
Brief Title
Continues Positive Airway Pressure Treatment for Patients With Dilated Cardiomyopathy and Obstructive Sleep Apnea
Acronym
RIDA
Official Title
Impact of Continues Positive Airway Pressure Treatment in Patients With Dilated Cardiomyopathy and Obstructive Sleep Apnea (RIDA)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Unknown status
Study Start Date
November 2014 (undefined)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
December 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Göteborg University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this randomized controlled study is to investigate the effect of continues positive airway pressure (CPAP) treatment in patients with dilated cardiomyopathy (DCM) and concomitant obstructive sleep apnea (OSA). The primary endpoint is left ventricular function measured by magnetic resonance (improvement of at least 4%) after six months treatment with CPAP. The secondary endpoints include diastolic dysfunction, cardiovascular biomarkers and quality of life.
Detailed Description
Sleep apnea, either obstructive (OSA) and central (CSA), occurs in more than half of all patients with heart failure (HF), and is associated with poor prognosis in these individuals. Dilated cardiomyopathy (DCM) is the most common type of cardiomyopathy and is defined as the presence of the left ventricle dilatation and left ventricular systolic dysfunction without concurrent valvular or coronary artery disease. Its etiology is unclear, but a genetic component is present in at least 25% of cases. In younger individuals, the etiology is more heterogeneous, where a rare type of cardiomyopathy may occur in women in connection with pregnancy, s.c. peripartum cardiomyopathy. Other underlying causes include alcohol, drugs, pharmaceuticals, endocrine disorders, systemic diseases and general muscle. These factors account for approximately half the cases of DCM in younger and other half designated as idiopathic (IDCM). The relationship between cardiomyopathies and OSA is insufficiently studied so far. In a smaller population of 20 individuals with DCM, sleep apnea (OSA or CSA) had 16, ie 80% of patients. The first-line treatment of OSA is continues positive pressure breathing mask (CPAP) during sleep in patients with daytime sleepiness. Effect of CPAP therapy in patients with DCM and OSA is completely unknown, because many of them do not report daytime sleepiness. The fact that patients with heart failure and reduced pumping function usually have symptoms of including fatigue, it becomes difficult to distinguish what is fatigue due to heart failure and what is related to sleep apnea. Interpretation of the Epworth Sleepiness Scale (ESS) is thus difficult and possibly unsure why all patients with DCM and OSA will be randomized to treatment with CPAP.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dilated Cardiomyopathy, Obstructive Sleep Apnea

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
44 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Continues Positive Airway Pressure
Arm Type
Experimental
Arm Description
Use of Continues Positive Airway Pressure (CPAP) mask every night under six months period.
Arm Title
Consultation of conservative measures
Arm Type
No Intervention
Arm Description
Study participants with DCM and OSA (no-CPAP), participants receive consultation of conservative measures such as avoiding alcohol before bedrest, sleeping on the side...
Intervention Type
Device
Intervention Name(s)
Continues Positive Airway Pressure (CPAP)
Intervention Description
Mask with positive airway pressure during exhalation which maintains the airway open
Primary Outcome Measure Information:
Title
Change in left ventricular ejection fraction (LVEF) six months after randomization to Continues Positive Airway Pressure (CPAP) treatment or consultation of conservative measures
Description
The primary endpoint is left ventricular ejection fraction (LVEF) measured by cardiac magnetic resonance (improvement of at least 4%) at study baseline and at 6 months after randomization to Continues Positive Airway Pressure (CPAP) or consultation of conservative measures.
Time Frame
6 months
Title
Change in left ventricular ejection fraction (LVEF) six months after randomization to Continues Positive Airway Pressure (CPAP) treatment or consultation of conservative measures
Description
The primary endpoint is left ventricular ejection fraction (LVEF) measured by echocardiography at study baseline and at 6 months after randomization to Continues Positive Airway Pressure (CPAP) or consultation of conservative measures.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Change in measurements of diastolic function after randomization to Continues Positive Airway Pressure (CPAP) or consultation of conservative measures.
Description
Secondary outcomes include measurements of diastolic function measured by cardiac magnetic resonance (CMR) and echocardiography,
Time Frame
baseline and at six months
Title
Change in measurements of cardiovascular biomarkers at
Description
Analyzing change in cardiovascular biomarkers by analyzing blood samples
Time Frame
baseline and at six months
Title
Change in quality of life questioners
Description
Analyzing participants response to quality of life by analyzing established questioners regarding dilated cardiomyopathy (Kansas city cardiomyopathy questionnaire KCCQ).
Time Frame
baseline and at six months
Title
Change in day-time sleepiness
Description
Analyzing participants respons to established questioners regarding sleep apnea (Epworth sleepiness scale ESS) and
Time Frame
baseline and at six month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with newly diagnosed or previously known DCM, treated and followed at cardiology outpatients clinic, stable in their symptoms and functional class at least 2 weeks after the last medicine change. Consent for the study. EF ≤ 45%. OSA diagnosis (Apnea-Hypopnea index> = 15 in the sleep recording below). Exclusion Criteria: Patients already treated with Continues Positive Airway Pressure. Patients with claustrophobia
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Maria Schaufelberger, Associate Professor
Phone
+46313434085
Email
maria.schaufelberger@gu.se
First Name & Middle Initial & Last Name or Official Title & Degree
Carmen Basic, MD
Phone
+46704807426
Email
carmen.basic@gu.se
Facility Information:
Facility Name
Sahlgrenska University Hospital/Östra
City
Gothenburg
ZIP/Postal Code
41678
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maria Schaufelberger, Assoc.Prof.
Phone
+46313434085
Email
maria.schaufelberger@gu.se
First Name & Middle Initial & Last Name & Degree
Carmen Basic, MD
Phone
+46704807426
Email
carmen.basic@gu.se
First Name & Middle Initial & Last Name & Degree
Erik Thunström, MD, PhD
First Name & Middle Initial & Last Name & Degree
Yuksel Peker, Professor

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Continues Positive Airway Pressure Treatment for Patients With Dilated Cardiomyopathy and Obstructive Sleep Apnea

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