Investigating a Wrist-sensor Oximeter to Screen for Sleep Apnoea.

UnknownOBSERVATIONAL
Enrollment

30

Participants

Timeline

Start Date

September 17, 2019

Primary Completion Date

December 17, 2019

Study Completion Date

December 17, 2019

Conditions
Obstructive Sleep Apnea
Interventions
DEVICE

Patient wears a wrist sensor oximeter device for one to two nights.

Patients will be asked to complete a study questionnaires of STOPBANG, SCI-8 (Sleep Condition Indicator-8 questionnaire for insomnia), Epworth questionnaires and medical history. The clinician will record blood pressure, pulse rate and regularity, body mass index and neck circumference. Subjects will be required to wear the wrist sensor pulse oximeter for 1-2 nights. The Oxitone 1000M device measures pulse rate, blood oxygen saturation and movement. The oxygen desaturation events from the wrist sensor device will be statistically compared with the diagnosis assessed using the conventional PPG oximetry, Peripheral Arterial Tonometry and clinical assessment. (clinicians will be masked when analysing the data from the wrist sensor pulse device).

Trial Locations (1)

W1G6BF

London Sleep Centre, London

Sponsors
All Listed Sponsors
collaborator

The London Sleep Centre

UNKNOWN

lead

Oxitone Medical Ltd.

INDUSTRY

NCT04018547 - Investigating a Wrist-sensor Oximeter to Screen for Sleep Apnoea. | Biotech Hunter | Biotech Hunter