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Not yet recruiting NCT07402603

Sleep-disordered Breathing Database

— Observational Obstructive Sleep Apnoea (OSA) Hypoventilation Syndrome

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Obstructive Sleep Apnoea (OSA), Hypoventilation Syndrome. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United Kingdom
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Enhancing Patient Care: Sleep and Ventilation Database

Overview

The goal of this study is to collect clinical data on patients who have had a sleep study and are given a diagnosis of a sleep related breathing disorder such as obstructive sleep apnoea. Collecting this data in an organised way will mean that the investigators can monitor patients and their health outcomes.

Detailed description

This is a prospective database collecting: symptom, physiological, comorbidity and treatment response data

Primary outcome measures

  • Number of patients consenting to participation in a database [Time frame: 5 years]
Secondary outcome measures (1)
  • Changes in symptoms and disease related variables [Time frame: 5 years initially, further ethical approval will be sought at 5 years to extend the database further]

Eligibility criteria

Inclusion criteria

  • Age >18 years
  • Referred to Royal Free London NHS Foundation Trust Sleep and Ventilation Service
  • Agreed to undertake a sleep study

Exclusion criteria

  • Inability to consent

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Other

Study locations

United Kingdom · 1 center
  • Royal Free London NHS Foundation Trust — London

Identifiers

NCT: NCT07402603 · 25-WS-0157

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗