Chronic Obstructive Pulmonary Disease (COPD) Clinical Trial
Official title:
Evaluation of Changes in Cardiac Function in COPD Patients With Resting Hyperinflation After Administration of Budesonide/Formoterol (Symbicort®) Compared With Placebo
To investigate whether Budesonide/Formoterol (Symbicort ®) therapy can improve heart function at rest by decreasing lung hyperinflation in patients with COPD (Chronic Obstructive Pulmonary Disease).
Patients with moderate to advanced COPD are known to have static hyperinflation (at rest) as
a consequence of expiratory flow limitation. Hyperinflation is easily detected by measuring
lung volumes during standard pulmonary function testing.
Decreased Inspiratory Capacity (IC) secondary to hyperinflation has been described as a
predictor of mortality in COPD, and as a limiting factor for the maximal tidal volume
attained during exercise. Hyperinflation has been linked to a low cardiac output in part by
limiting left ventricular ejection fraction during exercise.
Treatment with inhaled anticholinergic agents or long-acting beta agonists (LABA) and
combination of the LABA formoterol and budesonide has been shown to improve IC and decrease
lung hyperinflation. Bronchodilators have been shown to improve exercise endurance in COPD
when combined with pulmonary rehabilitation, however the exact mechanism: improvement of
lung mechanics and /or improvement in cardiac function is not well known.
Impedance cardiography (ICG) has emerged as a method to measure cardiac output without the
need for invasive devices. Cardiac output measurement by impedance cardiography (CO-ICG) is
a valid and reproducible method. It has been shown to have good correlation with
thermodilution and the direct Fick method for the measurement of stroke volume and cardiac
output.
In addition, the oxygen pulse, easily obtained by dividing the measured oxygen uptake by the
heart rate (VO2/HR) provides an adequate reflection of cardiac stroke volume when the
systemic extraction of oxygen is stable.
This method has been used to evaluate the effect of static and dynamic hyperinflation on
cardiac function.
This pilot study is designed to be a single center (Brigham and Women's Hospital),
randomized, placebo-controlled, double blind, crossover study of 14 patients (male and
female 40 to 80 years old) with COPD and static hyperinflation.
The primary endpoint is the measurement of stroke volume, cardiac output and oxygen pulse at
rest before and after the administration of budesonide/formoterol compared to placebo.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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