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Effect of preoperative screening and management on perioperative complications in patients with obstructive sleep apnea hypopnea syndrome

Effect of preoperative screening and management on perioperative complications in patients with obstructive sleep apnea hypopnea syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17013022
Enrollment
Unknown
Registered
2017-10-18
Start date
2017-10-18
Completion date
Unknown
Last updated
2017-10-23

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

Conditions

Obstructive sleep-apnea hypopnea syndrome

Interventions

Intervention group:Auto-CPAP

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. The patients scheduled to undergo elective surgery in our department of thoracic surgery; 2. aged 18~75 years old; 3. patients who are diagnosed as moderate to severe OSAHS by sleep monitoring in our hospital; 4. patients who agreed to participate in this study.

Exclusion criteria

Exclusion criteria: 1. patients who have contraindications to surgery; 2. patients who have severe lethargy (ESS> 15 points) and severe nocturnal hypoxemia (oxygen saturation 10% of recording time)or tidal breathing; 3. excluding patients who are pregnant and patients with lactation, puerperium and mental disorders; 4. excluding patients who have the recent application of hormones, sedatives or antipsychotic treatment; 5. patients who are accompanied by severe organic disease, significant memory, perception or behavioral disorders and life can not Self-care; 6. patients who are non-Chinese; 7. patients who are diagnosed as other sleep-disorderd breathing except OSAHS; 8. patients who have previous history of CPAP treatment or CPAP and APAP treatment contraindications; 9. patients who refused to PSG or whose EEG may be abnormal (Such as brain tumors, epilepsy and wearing deep brain stimulator, etc.); 10. patients who are participating in other clinical trials; 11. patients who are considered that they are not suitable for clinical trials by the researchers.

Design outcomes

Primary

MeasureTime frame
Perioperative complications;ICU stay time;Quality of life;Length of stay;

Secondary

MeasureTime frame
Anesthesia recovery time;Surgical risk classification;

Countries

China

Contacts

Public ContactNuofu Zhang

The First Affiliated Hospital of Guangzhou Medical University

nfzhanggird@163.com+86 13600460056

Outcome results

None listed

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