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Application of Portable Sleep Monitoring Parameters in Risk Prediction of Hypoxemia during Painless Gastrointestinal Endoscopy

Application of Portable Sleep Monitoring Parameters in Risk Prediction of Hypoxemia during Painless Gastrointestinal Endoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600125992
Enrollment
Unknown
Registered
2026-06-02
Start date
2025-11-23
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

Obstructive Sleep Apnea Syndrome

Interventions

Hypoxemia Group VS Non-hypoxemia Group:None

Sponsors

The First Affiliated Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1: Aged >= 18 years old; 2: American Society of Anesthesiologists (ASA) physical status classification I or II; 3: Good compliance; 4: Voluntary participation in the study and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1: A clear diagnosis of obstructive sleep apnea (OSA), or a history of receiving OSA treatment (e.g., continuous positive airway pressure [CPAP], tonsillectomy, uvulopalatopharyngoplasty [UPPP], tracheotomy); 2: Complicated with severe cardiovascular, cerebrovascular or pulmonary diseases, or with unstable hemodynamics; patients with chronic hypoxia (baseline peripheral oxygen saturation [SpO2] = III; 4: Patients taking sedative-hypnotic drugs; 5: Complicated with mental disorders or other special sleep disorders (e.g., periodic hypersomnia, narcolepsy, restless legs syndrome); 6: Failure to complete nocturnal monitoring or missing monitoring data.

Design outcomes

Primary

MeasureTime frame
Occurrence of Hypoxemia;Sleep breathing parameters;

Countries

China

Contacts

Public ContactXuezhao Cao

The First Affiliated Hospital of China Medical University

xzcao@cmu.edu.cn+86 138 8911 2202

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026