Alterations in Postprandial Glucose and Lipid Metabolism in Patients With Obstructive Sleep Apnea

NCT ID: NCT00942110

Last Updated: 2012-03-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

58 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-09-30

Study Completion Date

2012-03-31

Brief Summary

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The purpose of this study is to examine postprandial glucose and lipid metabolism in patients with obstructive sleep apnea.

Detailed Description

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Obstructive sleep apnea (OSA) is an increasingly prevalent condition that is characterized by repetitive upper airway obstructions. OSA has been independently associated with insulin resistance, suggesting that OSA may contribute to the development of type 2 diabetes and the metabolic syndrome. Recently, postprandial glucose and lipid have been reported as excellent predictors for mortality and cardiovascular risk. However, the association between postprandial glucose, lipid metabolism and OSA are not clear. In addition, humoral factors such as ghrelin and leptin are associated with obesity and OSA, but postprandial changes of which in patients with OSA are not well known. The aim of present study is to examine postprandial glucose and lipid metabolism, humoral factors in OSA before and after 3 months of continuous positive airway pressure (CPAP) treatment.

Conditions

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Obstructive Sleep Apnea

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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CPAP

Group Type EXPERIMENTAL

CPAP treatment

Intervention Type DEVICE

maintains upper airway patency and minimizes the obstructive events

Interventions

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CPAP treatment

maintains upper airway patency and minimizes the obstructive events

Intervention Type DEVICE

Other Intervention Names

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REMstar (Respironics), Auto Set(Resmed), Goodnight (Tyco Healthcare)

Eligibility Criteria

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Inclusion Criteria

* Subjects on admission for sleep study under the Respiratory Care and Sleep Control Medicine, Kyoto University Hospital.
* Subjects diagnosed with OSA (apnea hypopnea index \>=5/hour) by overnight polysomnography.

Exclusion Criteria

* Subjects treating for acute infections or malignancy.
* Subjects with severe anemia, diabetes,and renal failure.
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Kyoto University, Graduate School of Medicine

OTHER

Sponsor Role lead

Responsible Party

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Toru Oga

Medical doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Kazuo Chin, MD,PhD

Role: PRINCIPAL_INVESTIGATOR

Kyoto University, Graduate School of Medicine

Yuichi Chihara, MD,PhD

Role: PRINCIPAL_INVESTIGATOR

Kyoto University, Graduate School of Medicine

Locations

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Kyoto University Graduate School of Medicine

Kyoto, Kyoto, Japan

Site Status

Countries

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Japan

Other Identifiers

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C-311

Identifier Type: -

Identifier Source: org_study_id

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