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OpenTrials
Completed

NCT Number: NCT03122483

Use of Blood Biomarkers and Biomarker Index to Aid in the Diagnosis of Obstructive Sleep Apnea (OSA)

This multicenter prospective trial will evaluate the association between obstructive sleep apnea (OSA) and blood biomarkers in a representative population of consecutively enrolled symptomatic patients with a clinical suspicion of OSA.

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Key information

Age range

18 year–70 year

Sex eligibility

Male

Study type

Observational

Primary location

Sleep Center Orange County, Irvine, California, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Written Informed Consent
  • Male
  • 18-70 years old
  • Presentation with symptoms suggestive of obstructive sleep apnea
  • Diagnostic sleep study
  • Blood draw

Exclusion criteria

  • Prior (within past year) or current therapy for sleep apnea
  • Use of opioid pain medication, steroids or allopurinol (within past 30 days)
  • Use of chronic anti-inflammatory drugs (within past 7 days)
  • Active cancer under current treatment or monitoring

Treatment and study plan

blood biomarker

Diagnostic Test

Primary outcomes

  1. Identification of OSA in high-risk individuals

    Time frame: 1 day

    Identification of OSA in high-risk individuals

Sponsors and collaborators

Lead sponsor

Beckman Coulter, Inc.

Industry

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Apr 20, 2017
Registry last updated
Aug 18, 2017

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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