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Clinical Trials/NCT01136122
NCT01136122
Withdrawn
Not Applicable

Effects of Positive Airway Pressure (PAP) Treatment of Obstructive Sleep Apnea (OSA) in Patients With Heart Failure

Ulysses Magalang MD1 site in 1 country3 target enrollmentApril 1, 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obstructive Sleep Apnea
Sponsor
Ulysses Magalang MD
Enrollment
3
Locations
1
Primary Endpoint
Increase in circulating levels of adiponectin (Ad) and/or high-molecular-weight (HMW) Ad.
Status
Withdrawn
Last Updated
6 months ago

Overview

Brief Summary

The purpose of this study is to see if treatment of OSA with the CPAP device makes a difference to insulin resistance and heart disease.

Detailed Description

Obstructive Sleep Apnea (OSA) has been seen frequently in persons who develop insulin resistance and heart disease. Insulin resistance is a condition in which the body produces insulin but does not use it properly. Insulin helps the body use glucose for energy. Insulin resistance increases the chance of developing type II diabetes and heart disease. One method of treatment for OSA is with continuous positive airway pressure (CPAP). This treatment is given by a device named CPAP. There are many different types of CPAPs available on the market that are FDA approved. The purpose of this study is to see if treatment of OSA with the CPAP device makes a difference to insulin resistance and heart disease. This study will measure insulin resistance by testing the glucose level in the blood, and testing the levels of special protein found in blood, that are known to increase the sensitivity to insulin and decrease progression of heart disease. The heart disease will be measured by cardiac MRI. Glucose testing and cardiac MRI's are normal testing procedures for people who have OSA and heart disease, however will be conducted more frequently than normal and therefore are for research purposes. The specialized blood testing is for research purposes only.

Registry
clinicaltrials.gov
Start Date
April 1, 2010
End Date
October 1, 2013
Last Updated
6 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Ulysses Magalang MD
Responsible Party
Sponsor Investigator
Principal Investigator

Ulysses Magalang MD

Medical Director, Sleep Medicine-East

Ohio State University

Eligibility Criteria

Inclusion Criteria

  • 18 and \< 75 years of age.
  • Apnea-hypopnea index (AHI) of at least 15/hr based on overnight polysomnography.
  • New York Heart Association Class 3 or less.
  • LV ejection fraction \<45% based on a prior imaging study (as measured within one year of baseline studies).
  • Absence of exacerbation of heart failure requiring hospitalization within the previous 3 mos.
  • Optimal pharmacologic therapy at the highest tolerated dose \[3\].

Exclusion Criteria

  • Use of anti-diabetic medications
  • Primary valvular heart disease
  • Unstable angina
  • Myocardial infarction, cardiac surgery, or revascularization procedure within the previous 3 months
  • Uncontrolled hypertension defined as systolic blood pressure \>160 mm Hg or diastolic blood pressure \>100 mm Hg.
  • Active smoking (Patient should not have smoked for at least 1 month prior to baseline studies and has the intention not to smoke for the duration of the study period)
  • Use of illicit drugs
  • Current use of home oxygen therapy
  • Requirement for a bi-level machine to treat sleep apnea
  • Use of corticosteroids

Outcomes

Primary Outcomes

Increase in circulating levels of adiponectin (Ad) and/or high-molecular-weight (HMW) Ad.

Time Frame: One month

Secondary Outcomes

  • Increased levels of Ad and/or HMW Ad associate with improvements in insulin sensitivity and heart function in patients with known left ventricular (LV) systolic dysfunction.(One month)

Study Sites (1)

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