NCT06458777

Brief Summary

Obstructive sleep apnea (OSA) is a chronic pathology that affects more than 20% of the adult population. It is one of the main sleep disorders with great clinical, economic and social repercussions. To assess the impact and severity of obstructive sleep apnea, the number of apneas and hypopneas per hour (AHI) is counted. To define that a person has OAS, a sleep study must have an AHI ≥15/h, predominantly obstructive, or the presence of an AHI ≥5/h accompanied by symptoms. The diagnosis of certainty or exclusion, as well as the severity, is established with a sleep study. Polysomnography (PSG) continues to be the gold standard for the diagnosis of OSA, it encompasses the recording of cardiorespiratory and neurophysiological variables, which makes it possible to analyze sleep time and structure, the presence of different respiratory episodes and their repercussions. Respiratory polygraphy (RP) includes recording from a flow sensor, respiratory effort, oxygen saturation, heart rate, and also position but not EEG. There are several studies that have explored the diagnostic agreement of RP versus PSG, being a validated, useful and necessary test for the diagnosis of OSA in different clinical situations. Being cheaper and more accessible. When talking about the diagnosis of OSA, it refers to establishing whether or not there is, the severity and the therapeutic decision that will greatly affect the quality of life, prognosis and day-to-day life of the patient, since it is a chronic disease. It must be borne in mind that most studies are carried out in a field specialized in dream interpretation, so caution must be exercised in interpreting results in another field. PR teams incorporate increasingly better developed software that allows automatic analysis of records, but the technology and algorithms used vary depending on the device, and up to now the AASM continues to recommend manual analysis based on existing evidence. Several studies have examined the agreement between automatic and manual analysis of the PR record or between automatic analysis of PR and PSG. It seems that this agreement is reached above all in the highest AHIs, above 25-30, which may limit its use in clinical practice. For this reason, it is important to carry out a study with a large number of patients to achieve statistical significance, and strong conclusions that support normal clinical practice, and to disable a study that does not meet the scientific requirements when interpreting and reading.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
3,144

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2014

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 19, 2014

Completed
6.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 28, 2020

Completed
3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

March 15, 2023

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

August 2, 2023

Completed
11 months until next milestone

First Posted

Study publicly available on registry

June 14, 2024

Completed
Last Updated

June 20, 2024

Status Verified

June 1, 2024

Enrollment Period

6.2 years

First QC Date

August 2, 2023

Last Update Submit

June 17, 2024

Conditions

Outcome Measures

Primary Outcomes (2)

  • Evaluation of the Cost-Effectiveness and Sensitivity of Automatic Analysis Versus Manual Analysis of Polygraphy in the Diagnosis of Obstructive Sleep Apnea.

    effectiveness of the analysis described with the AHI (number of sleep apneas in each hour slept)

    2 years

  • Evaluation of the Cost-Effectiveness and Sensitivity of Automatic Analysis Versus Manual Analysis of Polygraphy in the Diagnosis of Obstructive Sleep Apnea.

    economic cost (measured in euros) of manual and automatic polygraphy

    2 years

Study Arms (2)

Patients diagnosed with manual report of polygraphy

Diagnostic Test: poligraphy

Patients diagnosed with automatical report of polygraphy

Diagnostic Test: poligraphy

Interventions

poligraphyDIAGNOSTIC_TEST

OSA diagnosis

Patients diagnosed with automatical report of polygraphyPatients diagnosed with manual report of polygraphy

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Dream Unit Patients with diagnostic suspicion of OSA

You may qualify if:

  • Respiratory polygraphs carried out at the San Pedro Hospital in the period of time between 2014-2020.
  • Polygraphs corresponding to patients over 18 years of age.

You may not qualify if:

  • Poor technical quality of polygraphy
  • Patients with \>50% central apnea or presence of Cheyne-Stokes respiration (CSResp).
  • Lack of automatic and/or manual analysis of the polygraph.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hospital San Pedro

Logroño, La Rioja, 26006, Spain

Location

MeSH Terms

Conditions

Sleep Apnea, Obstructive

Condition Hierarchy (Ancestors)

Sleep Apnea SyndromesApneaRespiration DisordersRespiratory Tract DiseasesSleep Disorders, IntrinsicDyssomniasSleep Wake DisordersNervous System Diseases

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 2, 2023

First Posted

June 14, 2024

Study Start

January 19, 2014

Primary Completion

March 28, 2020

Study Completion

March 15, 2023

Last Updated

June 20, 2024

Record last verified: 2024-06

Locations