A Prospective Study to Evaluate the WP in Comparison to PSG in Patients Suspected of Sleep Disorders
Recruiting now
Conditions studied: Sleep Disorder
In brief
The current study is a prospective blinded study to collect data regarding the performance of the WP device in detecting sleep disorders. For that purpose, the WP with finger probe and chest sensor will be worn by the subject simultaneous to PSG in a sleep study at the clinical sleep lab. A PSG system will be recording the PSG data.
Key facts
- Study ID
- NCT06093633
- Run by
- Itamar-Medical, Israel
- People needed
- 600
- Starts
- 2022-09-19
- Expected to finish
- 2025-10-01
- Last updated by the study team
- 2025-08-22
Who can join
Age: 12 and older, up to 99. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age between 12-99
- Subjects that are able to read understand and sign the informed consent form of the study or by parents of subjects that are less than 18 years of age that are referred to undergo an overnight sleep study in the clinical sleep laboratory
- Subjects suspected of having sleep disorders or with comorbidities relevant to central sleep apnea.
You may not qualify if…
- Permanent pacemaker: atrial pacing or VVI without sinus rhythm.
- Finger deformity that precludes adequate sensor appliance.
Where it is running
- Johns Hopkins Bayview Asthma and Allergy Center — Baltimore, Maryland, United States (enrolling)
- University of Maryland St. Joseph Medical Group, Pulmonary Care & Sleep Medicine — Towson, Maryland, United States (enrolling)
- Tel-Aviv Medical Center — Tel Aviv, Israel (enrolling)
Full record on ClinicalTrials.gov
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