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NCT01580085 Clinical Trial

Obstructive Sleep Apnea in Pulmonary Embolism

Obstructive Sleep Apnea Clinical Trial

Official title:
Obstructive Sleep Apnea is Prevalent in Patients With Pulmonary Embolism

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01580085
Other study ID # gantep gogus 1
Secondary ID
Status Completed
Phase N/A
First received April 16, 2012
Last updated April 17, 2012
Start date November 2009
Est. completion date December 2010

Study information
Verified date April 2012
Source University of Gaziantep
Contact n/a
Is FDA regulated No
Health authority Turkey: Ministry of Health
Study type Observational

Clinical Trial Summary

Obstructive sleep apnea (OSA) is a clinical syndrome characterized by repetitive closure of the airway and frequent awakenings during sleep. Repeated episodes of hypoxia, decrease in intrathoracic pressure, increased venous return and venous stasis, damage to vascular wall may ensue. An increased tendency for coagulation has also been reported in OSA. Venous stasis, vascular endothelial activation and hypercoagulability are also known risk factors for thromboembolism. All of these pathophysiologic changes in OSA may predispose patients for the development of pulmonary embolism (PE) however there is limited data about role of thromboembolic events in OSA.

Recruitment information / eligibility
Status Completed
Enrollment 75
Est. completion date December 2010
Est. primary completion date December 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- All consecutive patients diagnosed with pulmonary embolism

Exclusion Criteria:

- less than 18 years of age

- any restrictive or obstructive lung disease

Study Design

Observational Model: Case Control, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Intervention

Other:
• polysomnography
full night supervised laboratory polysomnography

Locations
Country Name City State
Turkey University of Gaziantep Hospital Gaziantep

Sponsors (1)
Lead Sponsor Collaborator
University of Gaziantep

Country where clinical trial is conducted

Turkey, 

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