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OpenTrials
Completed

NCT Number: NCT00768807

Structural and Functional Left Ventricular Remodelling in Patients With Obstructive Sleep Apnea

The purpose of this study is to determine whether patients with obstructive sleep apnea have any changes in left ventricular function and structure after 06 months of continuous positive airway pressure treatment.

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Key information

Age range

35 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Instituto do Sono/AFIP

São Paulo, 04516001, Brazil

About this study

Several studies have been suggesting that Obstructive Sleep Apnea contributes to deterioration of left ventricular diastolic function. It may be associated to increased risk of cardiovascular events. We hypothesized that morphological and functional left ventricular changes might be reverted after treatment with Continuous positive airway pressure.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Apnea-hypopnea index higher than 5 events per hour

Exclusion criteria

  • Body mass index higher than 40 kg/m2

Treatment and study plan

CPAP (continuous positive airway pressure)

Device

Patients treated by CPAP for 06 months

Primary outcomes

  1. Improvement of left ventricular diastolic echo variable

    Time frame: 06 months

Sponsors and collaborators

Lead sponsor

Associação Fundo de Incentivo à Pesquisa

Other

Registry information

Important dates

Study start
2009
Primary completion
2009
Study completion
2010
First posted
Oct 8, 2008
Registry last updated
May 8, 2012

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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