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Sleep Apnoea Breathing Record Exploratory Study (SABRES)

U

University Hospitals of North Midlands NHS Trust

Status

Active, not recruiting

Conditions

Sleep Apnea

Treatments

Device: Apne-Scan DC1 device

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

During sleep, many people have times when they breathe shallowly or completely stop. If a person stops breathing for more than 10 seconds, this is called an 'apnoea'. If shallow breathing lasts for more than 10 seconds, it is called a 'hypopnoea'. If a person has these events frequently, it disrupts their sleep and they do not awake refreshed. It can also put strain on the heart, leading to cardiovascular conditions. These sleep disorders, usually called 'Sleep Apnoea', can be treated for most people using 'continuous positive airways pressure', CPAP. Current tests for sleep apnoea, usually used at home, are expensive, complicated for patients to use and do not monitor actual breathing. The new test, called Apne-Scan, is very simple and will cost less than the standard tests. It just requires the user to wear a mask, similar to ones used for CPAP treatment, overnight and then send the mask off for data analysis. The Apne-Scan mask, developed with taxpayer funding, is fitted with a pressure sensor to monitor actual breathing. People between the ages of 18-70 who have been referred to the sleep clinic at Royal Stoke University Hospital are eligible to participate in this exploratory study. They will wear the Apne-Scan mask at the same time as their standard overnight sleep apnoea test. The breathing data collected by Apne-Scan will be analysed by Apnea-Tech Limited, the device manufacturers, so that it can be compared to the data captured by the standard sleep apnoea test.

Enrollment

39 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Have been referred by a clinician to the sleep clinic for diagnosis of a sleep disorder, possibly sleep apnoea.
  • Be about to be screened for possible sleep apnoea using a standard sleep apnoea test device.
  • Be between the ages of 18 and 75 and have provided informed consent for the study

Exclusion criteria

  • Have not been referred by a clinician to a sleep clinic for diagnostic tests for sleep disorders other than for possible sleep apnoea.
  • Cannot tolerate wearing a mask overnight.
  • Cannot remove a mask should they become distressed.
  • Are not capable of understanding the English language version of Apne-Scan's Instructions For Use (IFU).
  • Are under the age of 18 years old or over the age of 75 years old.
  • Are not capable of giving informed consent

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

39 participants in 1 patient group

Sleep disorder patients
Other group
Description:
The study participants have been referred by a clinician to the sleep clinic for diagnosis of a sleep disorder, possibly sleep apnoea.
Treatment:
Device: Apne-Scan DC1 device

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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