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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05570747
Other study ID # BSL-SNAP-001
Secondary ID 1R44HL158286-01A
Status Completed
Phase N/A
First received
Last updated
Start date October 19, 2022
Est. completion date November 11, 2022

Study information

Verified date January 2023
Source Bleep, LLC
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study is designed to assess the usability of a novel CPAP human interface compared to a traditional nasal mask. Human subjects will interact with two different CPAP interfaces including a traditional CPAP mask and the 2nd generation DreamPort-Eclipse. Subjects will be requested to put on each of the different CPAP interface options a total of three times for a total of 6 trials. The order of device will be randomized.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date November 11, 2022
Est. primary completion date November 11, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Male or female =18 years old who are impacted by obstructive sleep apnea and currently are familiar with a CPAP device. Exclusion Criteria: - Diagnosis of any medical or behavioral conditions that would compromise subject safety. - Under the age of 18: target for this current version of the platform is the adult population.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Eclipse novel CPAP mask
Participants will follow instructions to set up and put on the Eclipse nasal mask. The Eclipse removes the headgear associated with traditional CPAP masks, offering a small compact design weighing less than an ounce. The Eclipse uses small and lightweight adhesive seals around the nostrils to create an ergonomic design which accommodates the shape of each individual user. It completes a perfect circuit for CPAP therapy to deliver pressure to the airway and stabilize the user's disordered breathing during sleep (apnea and snoring). Participants will follow instructions to set up and put on the mask. They will fill out a survey about the ease and comfort of putting on and wearing the mask, briefly.
Phillips Respironics Nuance
Participants will follow instructions to set up and put on the Respironics Nuance, traditional nasal mask. Participants will follow instructions to set up and put on the mask. They will fill out a survey about the ease and comfort of putting on and wearing the mask, briefly.

Locations

Country Name City State
United States AeroFlow Sleep Asheville North Carolina
United States Advanced Respiratory and Sleep Medicine Huntersville North Carolina
United States Sleep Centers of Middle Tennessee Murfreesboro Tennessee

Sponsors (2)

Lead Sponsor Collaborator
Bleep, LLC National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time to complete each setup Investigators will record the time it takes the participant to set up and try on each device. 1 day
Primary Number of technical issues Investigators will record the number of observed technical issues that occurred when the participant attempts to set up and try on the device. 1 day
Primary Number of times participant needs assistance Investigators will record the number of times each participant requires assistance or additional instructions setting up and trying on each device. 1 day
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