Skip to content

Millimetre wave radar-based non-contact sleep apnea monitoring measurement in children with OSAS

Millimetre wave radar-based non-contact sleep apnea monitoring measurement in children with OSAS

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400081367
Enrollment
Unknown
Registered
2024-02-29
Start date
2024-03-01
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Obstructive sleep apnea in Children

Interventions

Gold Standard:Results of polysomnography suggesting an OAHI (Obstructive Sleep Apnoea Hypopnoea Index) of >1/hour is diagnostic of OSAS in children.
Index test:Millimetre-wave radar-based non-contact sleep apnea monitoring device

Sponsors

Shanghai Children's Medical Center Affiliated to Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 18 Years

Inclusion criteria

Inclusion criteria: (1) Male or female children aged 1 to 18 years; (2) Having symptoms of nighttime snoring, breath-holding, apnea or open-mouth breathing from March 2024 to December 2024, and undergoing all-night polysomnography at the Shanghai Children's Medical Centre; (3) Informed consent for the study was obtained from the legal guardians of the children (children over 8 years of age were also required to give their informed consent).

Exclusion criteria

Exclusion criteria: (1) Presence of chronic lung disease, congenital heart disease, chronic liver or kidney disease, neuromuscular disease, inherited metabolic disease, chromosomal or genetic abnormalities, craniofacial developmental malformations, and any other underlying disease; (2) Those undergoing non-invasive positive pressure ventilation; (3) Those who may have other sleep disorders as assessed clinically; (4) Those who have obtained less than 6 hours of polysomnography sleep monitoring; (5) The sleep technician has reviewed and confirmed that the acquired polysomnography data are not adequate for analysis; (6) The investigator believes that the subject is at potential risk or has any other factors that interfere with the subject's ability to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
Obstructive apnea hypopnea index;

Countries

China

Contacts

Public ContactJing Zhang

Shanghai Children's Medical Center Affiliated to Shanghai Jiao Tong University School of Medicine

zhangjing@scmc.com.cn+86 139 1713 9575

Outcome results

None listed

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