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Recruiting NCT06334640

Sleeping Quality and Chronic Ocular Diseases

Observational Sleep Disorder

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
The protocol lists: Three questionaires.
Who it may be relevant to
Registry conditions: Sleep Disorder. 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
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

L'Impatto Del Sonno Nelle Patologie Croniche Oculari

Overview

To assess the impact of sleep quality on chronic eyes diseases

Detailed description

In this study 3 questionnaires will be distributed to outpatients attending the routine examinations : the Pittsburgh, the Berlin and the Epworth tests These questionnaires, once completed, will then be collected to be then transformed into digital files for the appropriate statistical evaluations and the drafting of the results and conclusions.

Interventions

  • Diagnostic test Three questionaires
    Berlin, Pittsburgh and Epworth tests administered during study visit

Primary outcome measures

  • Proportion of sleep disorders in patients and healthy volunteers [Time frame: At enrollment]

Eligibility criteria

Inclusion criteria

  • Patients with macular degeneration or glaucoma or
  • Healthy volunteers

Exclusion criteria

\- Patients with other ocular disorders

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
Cohort

Study locations

Italy · 1 center
  • Istituto Auxologico Italiano IRCCS — Milan

Identifiers

NCT: NCT06334640 · 37C302

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗