PASHOS Project: Advanced Platform for Sleep Apnea Syndrome Assessment

Overview

The purpose of this study is to develop and validate a work-model in Primary Health Care for identifying patients with Sleep Apnea Syndrome, based on clinical variables and an ambulatory monitoring study.

Full Title of Study: “PASHOS Project: Advanced Platform for Sleep Apnea Syndrome Assessment. A Multi-Centre Study to Validate a Sleep Apnea Screening Model in Primary Health Care”

Study Type

  • Study Type: Observational [Patient Registry]
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: October 2018

Clinical Trial Outcome Measures

Primary Measures

  • Apnea/Hypopnea Index
    • Time Frame: At baseline
    • At primary healthcare
  • Apnea/Hypopnea Index
    • Time Frame: At 3 months
    • At Sleep Lab Unit

Secondary Measures

  • Cardiovascular risk factors
    • Time Frame: At baseline
  • History of cardiovascular or cerebrovascular disease
    • Time Frame: At baseline
  • Lung function tests
    • Time Frame: At baseline
  • Self-perceived sleepiness. Epworth Test
    • Time Frame: At baseline
    • At primary healthcare
  • Self-perceived sleepiness. Epworth Test
    • Time Frame: At 3 months
    • At Sleep lab unit

Participating in This Clinical Trial

Inclusion Criteria

  • Patients between 18 to 75 years. Exclusion Criteria:

  • Cognitive impairment or psycho-physical deterioration that impede to perform ambulatory monitoring study. – Worsened or unstable cardiovascular or cerebrovascular disease. – Chronic insomnia (<5h sleep / day). – Relevant respiratory comorbidity that could interfere with arterial saturation measurements, as moderate to severe chronic obstructive pulmonary disease. – Neuromuscular disease. – Refusal to participate in the study.

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: 75 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Fundació Institut de Recerca de l’Hospital de la Santa Creu i Sant Pau
  • Provider of Information About this Clinical Study
    • Sponsor

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