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Completed

NCT Number: NCT02244957

Right Ventricular Hemodynamics Using Cardiac MRI in Patients COPD and OSA

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.

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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Bi-level positive airway pressure (BPAP)

Device

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.

Other names: BPAP

Nocturnal oxygen

Drug

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.

Other names: NOT

Primary outcomes

  1. Right Ventricular Remodeling Index

    Time frame: Six months

    Defined as the ratio between RVMI and RV end-diastolic volume index using MRI

Secondary outcomes

  1. Right Ventricular Mass Index

    Time frame: Six months

    MRI

  2. Right Ventricular End Systolic and Diastolic Volume

    Time frame: Six months

    MRI

  3. Right Ventricular Ejection Fraction

    Time frame: Six months

    MRI

  4. Myocardial Extracellular Volume

    Time frame: Six months

    MRI

  5. Left Ventricular Remodeling Index

    Time frame: Six months

    MRI

  6. Left Ventricular Mass Index

    Time frame: Six months

    MRI

  7. Left Ventricular End Systolic and Diastolic Volume

    Time frame: 6 months

    MRI

  8. Left Ventricular Ejection Fraction

    Time frame: 6 months

    MRI

  9. Serum C-reactive Protein Level

    Time frame: 6 months

    blood test

  10. Serum Tumor Necrosis Factor-alpha Level

    Time frame: 6 months

    blood test

  11. Serum Interleukin-6 Level

    Time frame: 6 months

    blood test

  12. Serum Intercellular Adhesion Molecule-1

    Time frame: 6 months

    blood test

  13. Serum P-selectin Level

    Time frame: 6 months

    Blood test

  14. Urine Catecholamine Level

    Time frame: 6 months

    Urine test

  15. 6 Minute Walk Distance

    Time frame: 6 months

    Low-grade physical activity test

  16. Quality of Life Score Through St. George's Respiratory Questionnaire (SGRQ)

    Time frame: 6 months

    Questionnaire

  17. Degree of Daytime Sleepiness Through Epworth Sleepiness Scale (ESS)

    Time frame: 6 months

    Questionnaire

  18. Sleep Quality Through Pittsburgh Sleep Quality Index (PSQI)

    Time frame: 6 months

    Questionnaire

  19. General Health Status Through Short Form 36 (SF-36) Health Survey

    Time frame: 6 months

    Questionnaire

Sponsors and collaborators

Lead sponsor

University of California, San Diego

Other

Registry information

Official study title

Right Ventricular Hemodynamics Using Cardiac Magnetic Resonance Imaging in Patients With Chronic Obstructive Pulmonary Disease (COPD) and Obstructive Sleep Apnea (OSA)

Important dates

Study start
2014
Primary completion
2017
Study completion
2020
First posted
Sep 19, 2014
Registry last updated
Jul 28, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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