Right Ventricular Hemodynamics Using Cardiac MRI in Patients COPD and OSA
Primary Purpose
Obstructive Sleep Apnea, Chronic Obstructive Pulmonary Disease, Overlap Syndrome
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Bi-level positive airway pressure (BPAP)
Nocturnal oxygen
Sponsored by
About this trial
This is an interventional treatment trial for Obstructive Sleep Apnea
Eligibility Criteria
Inclusion Criteria:
- Both men and women with age more than 18 years.
- Known diagnosis of stable COPD (GOLD stage 2 or higher) or OSA.
Exclusion Criteria:
- Already using continuous positive airway pressure (CPAP), BPAP device, or nocturnal oxygen.
- Known or suspected renal failure with estimated Glomerular filtration (GFR) <50 ml/min/1.73 m2 or serum creatinine > 1.5 mg/dl.
- Chronic atrial fibrillation or frequent premature ventricular contraction (> 10 beats per hour)
- Women known to be pregnant or planning to be pregnant in next 6 months.
- Known contraindication to MRI: cardiac pacemaker, metallic heart valves, metallic implants, history of claustrophobia.
- If taking sildenafil or related drugs, unable to stop it within 48 hours of the study visit.
- Uncontrolled COPD or acute COPD exacerbation.
- Unstable cardiac diseases.
- Known chronic inflammatory diseases like lupus or active infection.
Sites / Locations
- University of California, San Diego
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Bi-level positive airway pressure (BPAP)
Nocturnal oxygen
Arm Description
Bi-level positive airway pressure (BPAP)
Nocturnal oxygen
Outcomes
Primary Outcome Measures
Right Ventricular Remodeling Index
Defined as the ratio between RVMI and RV end-diastolic volume index using MRI
Secondary Outcome Measures
Right Ventricular Mass Index
MRI
Right Ventricular End Systolic and Diastolic Volume
MRI
Right Ventricular Ejection Fraction
MRI
Myocardial Extracellular Volume
MRI
Left Ventricular Remodeling Index
MRI
Left Ventricular Mass Index
MRI
Left Ventricular End Systolic and Diastolic Volume
MRI
Left Ventricular Ejection Fraction
MRI
Serum C-reactive Protein Level
blood test
Serum Tumor Necrosis Factor-alpha Level
blood test
Serum Interleukin-6 Level
blood test
Serum Intercellular Adhesion Molecule-1
blood test
Serum P-selectin Level
Blood test
Urine Catecholamine Level
Urine test
6 Minute Walk Distance
Low-grade physical activity test
Quality of Life Score Through St. George's Respiratory Questionnaire (SGRQ)
Questionnaire
Degree of Daytime Sleepiness Through Epworth Sleepiness Scale (ESS)
Questionnaire
Sleep Quality Through Pittsburgh Sleep Quality Index (PSQI)
Questionnaire
General Health Status Through Short Form 36 (SF-36) Health Survey
Questionnaire
Full Information
NCT ID
NCT02244957
First Posted
September 15, 2014
Last Updated
July 13, 2020
Sponsor
University of California, San Diego
1. Study Identification
Unique Protocol Identification Number
NCT02244957
Brief Title
Right Ventricular Hemodynamics Using Cardiac MRI in Patients COPD and OSA
Official Title
Right Ventricular Hemodynamics Using Cardiac Magnetic Resonance Imaging in Patients With Chronic Obstructive Pulmonary Disease (COPD) and Obstructive Sleep Apnea (OSA)
Study Type
Interventional
2. Study Status
Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
September 2014 (undefined)
Primary Completion Date
February 2017 (Actual)
Study Completion Date
February 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, San Diego
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The coexistence of chronic obstructive pulmonary disease (COPD) and obstructive sleep apnea (OSA) in the same patient has been termed overlap syndrome, affecting 1% of the U.S. population.The investigators propose to conduct this study that aims: (1) to compare right and left ventricular hemodynamic parameters using cardiac magnetic resonance imaging (MRI) in overlap syndrome vs. COPD only and OSA only; (2) to compare the effects of bi-level positive airway pressure (BPAP) vs. nocturnal oxygen therapy (NOT) on right ventricular (RV) hemodynamics in overlap syndrome.
This study will allow us to test the hypothesis: (1) Patients with overlap syndrome have more RV dysfunction than those with COPD only or OSA only; (2) treatment of both hypoxemia and hypercapnia during sleep will improve RV hemodynamics compared with treatment of hypoxemia alone in patients with overlap syndrome.
Detailed Description
Despite the high prevalence of overlap syndrome, few data are available on its pathophysiology and clinical consequences of these patients. Overlap syndrome has recently been reported to have excess cardiovascular mortality compared with COPD alone. However, no study has evaluated the mechanisms of excess cardiovascular mortality in untreated overlap syndrome. In addition, no prospective, randomized, controlled data are currently available on treatment of overlap syndrome.
This study is divided into two parts. The first part (Part 1) is a cross-sectional cohort study comparing subjects with overlap syndrome to those with COPD alone and those with OSA alone. Patients with COPD and OSA overlap syndrome will be evaluated by an overnight sleep study, cardiac MRI, serum inflammatory biomarker, urine catecholamine level, pulmonary function test, and questionnaires of sleep and health related quality of life. These measurement will be compared between overlap syndrome and control groups with either COPD or OSA alone.
The second part (Part 2) of the study is a prospective, parallel-group, randomized, controlled pilot study examining the effect of BPAP (and nocturnal oxygen if needed) vs. nocturnal oxygen therapy alone in patients with overlap syndrome (20 subjects in each treatment arm). The same measurement done during Part 1 will be repeated to evaluate the treatment effects.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obstructive Sleep Apnea, Chronic Obstructive Pulmonary Disease, Overlap Syndrome
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
23 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Bi-level positive airway pressure (BPAP)
Arm Type
Active Comparator
Arm Description
Bi-level positive airway pressure (BPAP)
Arm Title
Nocturnal oxygen
Arm Type
Active Comparator
Arm Description
Nocturnal oxygen
Intervention Type
Device
Intervention Name(s)
Bi-level positive airway pressure (BPAP)
Other Intervention Name(s)
BPAP
Intervention Description
Overlap patients randomized to BPAP will be titrated as per American Academy of Sleep Medicine (AASM) guidelines and oxygen if needed based on saturations <88% while on stable bi-level settings.
Intervention Type
Drug
Intervention Name(s)
Nocturnal oxygen
Other Intervention Name(s)
NOT
Intervention Description
Oxygen will be titrated to keep resting oxygen saturation (as measured by pulse oximeter) more than 88 percent. The duration of therapy will be six months.
Primary Outcome Measure Information:
Title
Right Ventricular Remodeling Index
Description
Defined as the ratio between RVMI and RV end-diastolic volume index using MRI
Time Frame
Six months
Secondary Outcome Measure Information:
Title
Right Ventricular Mass Index
Description
MRI
Time Frame
Six months
Title
Right Ventricular End Systolic and Diastolic Volume
Description
MRI
Time Frame
Six months
Title
Right Ventricular Ejection Fraction
Description
MRI
Time Frame
Six months
Title
Myocardial Extracellular Volume
Description
MRI
Time Frame
Six months
Title
Left Ventricular Remodeling Index
Description
MRI
Time Frame
Six months
Title
Left Ventricular Mass Index
Description
MRI
Time Frame
Six months
Title
Left Ventricular End Systolic and Diastolic Volume
Description
MRI
Time Frame
6 months
Title
Left Ventricular Ejection Fraction
Description
MRI
Time Frame
6 months
Title
Serum C-reactive Protein Level
Description
blood test
Time Frame
6 months
Title
Serum Tumor Necrosis Factor-alpha Level
Description
blood test
Time Frame
6 months
Title
Serum Interleukin-6 Level
Description
blood test
Time Frame
6 months
Title
Serum Intercellular Adhesion Molecule-1
Description
blood test
Time Frame
6 months
Title
Serum P-selectin Level
Description
Blood test
Time Frame
6 months
Title
Urine Catecholamine Level
Description
Urine test
Time Frame
6 months
Title
6 Minute Walk Distance
Description
Low-grade physical activity test
Time Frame
6 months
Title
Quality of Life Score Through St. George's Respiratory Questionnaire (SGRQ)
Description
Questionnaire
Time Frame
6 months
Title
Degree of Daytime Sleepiness Through Epworth Sleepiness Scale (ESS)
Description
Questionnaire
Time Frame
6 months
Title
Sleep Quality Through Pittsburgh Sleep Quality Index (PSQI)
Description
Questionnaire
Time Frame
6 months
Title
General Health Status Through Short Form 36 (SF-36) Health Survey
Description
Questionnaire
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Both men and women with age more than 18 years.
Known diagnosis of stable COPD (GOLD stage 2 or higher) or OSA.
Exclusion Criteria:
Already using continuous positive airway pressure (CPAP), BPAP device, or nocturnal oxygen.
Known or suspected renal failure with estimated Glomerular filtration (GFR) <50 ml/min/1.73 m2 or serum creatinine > 1.5 mg/dl.
Chronic atrial fibrillation or frequent premature ventricular contraction (> 10 beats per hour)
Women known to be pregnant or planning to be pregnant in next 6 months.
Known contraindication to MRI: cardiac pacemaker, metallic heart valves, metallic implants, history of claustrophobia.
If taking sildenafil or related drugs, unable to stop it within 48 hours of the study visit.
Uncontrolled COPD or acute COPD exacerbation.
Unstable cardiac diseases.
Known chronic inflammatory diseases like lupus or active infection.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert L Owens, MD
Organizational Affiliation
UCSD
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, San Diego
City
San Diego
State/Province
California
ZIP/Postal Code
92093
Country
United States
12. IPD Sharing Statement
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Right Ventricular Hemodynamics Using Cardiac MRI in Patients COPD and OSA
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