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Clinical trial of polysomnography

A Multicenter, Open-Labeled, Self-Paired Study to Examine the Effectiveness, Safety and Operability of a Portable Sleep Monitor Device

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900023832
Enrollment
Unknown
Registered
2019-06-13
Start date
2018-10-30
Completion date
Unknown
Last updated
2019-06-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

sleep disorder

Interventions

Gold Standard:traditional polysomnography (Trackit-32/0)
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Zhejiang&#32
Neurons&#32
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Co.,&#32
Ltd.

Sponsors

Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Aged between 18 to 65 years. Prescribed with polysomnogrphy for all-night sleep at our center.

Exclusion criteria

Exclusion criteria: Patients with restless leg syndrome, periodic leg movement, epilepsy, schizophrenia, sleepwalking, pregnancy, significant morbidities, electric devices implanted, pace maker, head injury were excluded. Patients who currently enrolled in other clinical trials, or patients who can not cooperate were also excluded from the study.

Design outcomes

Primary

MeasureTime frame
EEG;EOG;EMG;—

Secondary

MeasureTime frame
Nasal-oral Air Flow;Chest breathing exercise;Oxygen saturation;Pulse rate;—

Countries

China

Contacts

Public ContactXingyue Hu

Run Run Shaw Hospital, College of Medicine, Zhejiang University

sunyingying@neurons.top+86 13805736386

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026