Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
186 participants
OBSERVATIONAL
2023-10-17
2025-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Evaluation of the Reliability and Validity of a Diagnostic Sleep Disorders Questionnaire
NCT03468400
Intervention and Effect of Sleep Pattern on Cardio-cerebrovascular Disease
NCT06294964
Long-term Observation of Ophthalmic Changes in Patients With Obstructive Sleep Apnea
NCT03928665
The Role of the Circadian System in Neurological Sleep-wake Disorders
NCT03356938
Aging, Sleep, Cognitive Process
NCT00804804
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Subjects with glaucoma and macular degeneration
Adults subjects affected by glaucoma and macular degeneration
Three questionaires
Berlin, Pittsburgh and Epworth tests administered during study visit
Healthy volunteers
Adult healthy volunteers without eye disease
Three questionaires
Berlin, Pittsburgh and Epworth tests administered during study visit
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Three questionaires
Berlin, Pittsburgh and Epworth tests administered during study visit
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Healthy volunteers
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Istituto Auxologico Italiano
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Istituto Auxologico Italiano IRCCS
Milan, , Italy
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Paolo Milani, MD
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
37C302
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.