Sleep data acquisition and sleep apnea detection with low-power Doppler radar technology

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00023701

Enrollment

500

Registered

2021-01-04

Start date

2020-12-04

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

G47.3

Interventions

Group 1: Patients who receive a PSG examination as part of a diagnostic procedure in case of suspected sleep apnea or as part of the therapy control with already treated OSA are asked to participate.

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Presence of a signed and dated informed patient consent form for participation in the study Patients suspected os suffering from sleep-related respiratory who are scheduled for a diagnostic polysomnography or patients undergoing a. polysomnography for a purpose of positive pressure therapy monitoring

Exclusion criteria

Exclusion criteria: Pregnancy Implanted devices (e.g. pacemakers) Inability to sign the informed consent

Design outcomes

Primary

Measure	Time frame
Measurement of the standard sleep parameters using Doppler radar technology and comparison with parameters obtained with polysomnography	—

Secondary

Measure	Time frame
Correlation of the measured parameters to biometric data	—

Countries

Germany

Contacts

Public ContactFrank Käßner

Ambulantes Zentrum für Lungenkrankheiten und Schlafmedizin Cottbus - Schlaflabor im Carl-Thiem-Klinikum

post@lunge-schlaf.de0355 - 543 922

Outcome results

None listed

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