A Prospective Study to Evaluate the WP in Comparison to PSG in Patients Suspected of Sleep Disorders
NCT06093633
This study is recruiting at 2 US sites in 1 state, according to its ClinicalTrials.gov record last updated .
Summary
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.
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Sleep Disorder
Eligibility basics and study details
- Study type
- Observational
- Phase
- Not applicable
- Ages
- 12 to 99 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Sponsor
- Itamar-Medical, Israel
- Last updated on ClinicalTrials.gov
- August 22, 2025
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
Maryland · 2
- Johns Hopkins Bayview Asthma and Allergy Center · Baltimore, MD
- University of Maryland St. Joseph Medical Group, Pulmonary Care & Sleep Medicine · Towson, MD
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.