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Right Ventricular Hemodynamics Using Cardiac MRI in Patients COPD and OSA

University of California San Diego logo

University of California San Diego

Status

Completed

Conditions

Overlap Syndrome
Chronic Obstructive Pulmonary Disease
Obstructive Sleep Apnea

Treatments

Device: Bi-level positive airway pressure (BPAP)
Drug: Nocturnal oxygen

Study type

Interventional

Funder types

Other

Identifiers

NCT02244957
UCSD140959

Details and patient eligibility

About

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.

Full 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.

Enrollment

23 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

23 participants in 2 patient groups

Bi-level positive airway pressure (BPAP)
Active Comparator group
Description:
Bi-level positive airway pressure (BPAP)
Treatment:
Device: Bi-level positive airway pressure (BPAP)
Nocturnal oxygen
Active Comparator group
Description:
Nocturnal oxygen
Treatment:
Drug: Nocturnal oxygen

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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