RecruitingSleep Disorder
A Prospective Study to Evaluate the WP in Comparison to PSG in Patients Suspected of Sleep Disorders
Eligible age
12–99 yrs
Accepts
All genders
Locations
1 state
Healthy volunteers
No
See if you qualify for this study
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About this study
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.
Sponsor: Itamar-Medical, Israel
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's recruiting
Maryland
Baltimore · Towson
Source: ClinicalTrials.gov · NCT06093633 · last updated 2025-08-22