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Clinical Trials/ChiCTR2500111489
ChiCTR2500111489Not yet recruitingNot Applicable

术后持续气道正压通气改善阻塞性睡眠呼吸暂停患者认知功能的随机对照研究

自筹1 site in 1 country100 target enrollmentStarted: August 1, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
100
Locations
1
Primary Endpoint
神经损伤标志物 S100β

Study Overview

Brief Summary

评估在术后恢复室这一关键过渡期立即启动持续气道正压通气(CPAP)治疗,能否有效改善阻塞性睡眠呼吸暂停(OSA)患者行悬雍垂、腭咽成形术(UPPP)术后早期窗口期的认知功能表现。

Study Design

Study Type
干预性研究
Primary Purpose
随机平行对照
Masking

Eligibility Criteria

Ages
18 to 65 (—)
Sex
All

Inclusion Criteria

  • 在门诊手术室进行 UPPP 手术的 OSA 患者 2) ASA 分级Ⅲ级 3) 年龄 18-65 岁

Exclusion Criteria

  • 合并严重脏器功能损害 2) 伴有精神障碍等疾病及本人或家属拒绝入组

Arms & Interventions

CPAP 组

术后持续正压通气

非 CPAP 组

术后吸氧

Outcomes

Primary Outcomes

神经损伤标志物 S100β

蒙特利尔认知评估量表

护理谵妄筛查量表

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
自筹

Study Sites (1)

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